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Medicamento sin receta

Paracetamol, dextrometorfano y triprolidina (acetaminophen, dextromethorphan and triprolidine)

Propósito en la etiqueta: Pain reliever/fever reducer Cough suppressant Antihistamine

Tos, resfriado y gripe

Datos oficiales de la FDA, no son consejos

El texto de la etiqueta se cita exactamente como la empresa lo presentó a la Administración de Alimentos y Medicamentos de los EE. UU. (FDA), con un enlace a la copia oficial; se muestra en inglés. La lista de marcas viene del directorio NDC de la FDA.

Esta página no es un consejo médico. Lea la etiqueta de su envase y pregunte a un farmacéutico o médico si no está seguro de que un medicamento sea adecuado para usted, para su hijo o con sus otros medicamentos.

Si alguien pudo haber tomado demasiado, llame a la Línea de Ayuda para Envenenamientos (Poison Help): 1‑800‑222‑1222. En una emergencia, llame al 911.

Respuestas rápidas

¿Para qué se usa Paracetamol, dextrometorfano y triprolidina?
La etiqueta «Drug Facts» de Overnight Cold and Flu (Raritan Pharmaceuticals) indica estos usos, en inglés: temporarily relieves these common cold and flu symptoms: cough; minor aches and pains; sore throat; headache; runny nose; sneezing; itching of the nose or throat; itchy, watery eyes due to hay fever; temporarily reduces fever; controls cough to help you get to sleep.
¿Necesito receta para Paracetamol, dextrometorfano y triprolidina?
No. Los productos de esta página se venden sin receta.
¿Una marca de tienda es igual que la marca conocida?
Los productos que aparecen juntos abajo tienen los mismos principios activos, en la misma cantidad y la misma forma, según su registro ante la FDA. Los ingredientes inactivos (colorantes, sabores, rellenos) y el tamaño del envase pueden variar. Compare el recuadro «Active ingredient» de ambos envases y pregunte a un farmacéutico si tiene dudas.
¿Se ha retirado del mercado Paracetamol, dextrometorfano y triprolidina?
Los informes de la FDA indican 1 retiro de productos de esta página; el más reciente comenzó el 15 de abril de 2015. Un retiro suele afectar a productos o lotes concretos, no a todas las marcas.

Etiqueta «Drug Facts»

Todo medicamento sin receta debe llevar un recuadro «Drug Facts» con el mismo orden, fijado por las normas de la FDA. Abajo está la etiqueta de un producto por cada concentración y forma común, citada palabra por palabra (en inglés). Su envase puede ser distinto (por ejemplo, los productos para niños tienen otras instrucciones): siga siempre la etiqueta de su envase.

Overnight Cold and Flu · Raritan Pharmaceuticals

Acetaminophen 650 mg/20 mL · Dextromethorphan hydrobromide 20 mg/20 mL · Triprolidine hydrochloride 2.5 mg/20 mL, solución (oral)

Principio activo (in each 20 mL)

Purposes Acetaminophen 650 mg Pain reliever/fever reducer Dextromethorphan HBr 20 mg Cough suppressant Triprolidine HCl 2.5 mg Antihistamine

Propósito

Active ingredients (in each 20 mL) Purposes Acetaminophen 650 mg Pain reliever/fever reducer Dextromethorphan HBr 20 mg Cough suppressant Triprolidine HCl 2.5 mg Antihistamine

Usos

  • temporarily relieves these common cold and flu symptoms:
  • cough
  • minor aches and pains
  • sore throat
  • headache
  • runny nose
  • sneezing
  • itching of the nose or throat
  • itchy, watery eyes due to hay fever
  • temporarily reduces fever
  • controls cough to help you get to sleep

Advertencias

Liver warning This product contains acetaminophen. Severe liver damage may occur if you take:

  • more than 4000 mg in 24 hours, which is the maximum daily amount
  • with other drugs containing acetaminophen
  • 3 or more alcoholic drinks daily while using this product Allergy alert Acetaminophen may cause severe skin reactions. Symptoms may include:
  • skin reddening
  • blisters
  • rash If a skin reaction occurs, stop use and seek medical help right away. Sore throat warning If sore throat is severe, persists for more than 2 days, is accompanied or followed by fever, headache, rash, nausea, or vomiting, consult a doctor promptly.

Do not use (No use)

  • with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist.
  • if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric, or emotional conditions, or Parkinson's disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product.

Ask a doctor before use if (Consulte a un médico antes de usar si)

you have

  • liver disease
  • glaucoma
  • trouble urinating due to an enlarged prostate gland
  • a breathing problem such as emphysema or chronic bronchitis
  • persistent or chronic cough such as occurs with smoking, asthma, or emphysema
  • cough that occurs with too much phlegm (mucus)

Ask a doctor or pharmacist before use if (Consulte a un médico o farmacéutico antes de usar si)

you are

  • taking the blood thinning drug warfarin
  • taking sedatives or tranquilizers

When using this product (Al usar este producto)

  • do not use more than directed
  • excitability may occur, especially in children
  • marked drowsiness may occur
  • alcohol, sedatives, and tranquilizers may increase drowsiness
  • avoid alcoholic drinks
  • use caution when driving a motor vehicle or operating machinery

Stop use and ask a doctor if (Deje de usarlo y consulte a un médico si)

  • pain or cough gets worse or lasts more than 7 days
  • fever gets worse or lasts more than 3 days
  • redness or swelling is present
  • new symptoms occur
  • cough comes back, or occurs with fever, rash, or headache that lasts. These could be signs of a serious condition.

If pregnant or breast-feeding (Si está embarazada o amamantando)

ask a health professional before use.

Keep out of reach of children (Mantener fuera del alcance de los niños)

Overdose warning Taking more than the recommended dose (overdose) may cause liver damage. In case of overdose, get medical help or contact a Poison Control Center right away. Quick medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.

Instrucciones

  • do not take more than directed (see Overdose warning )
  • do not take more than 4 doses in any 24-hour period
  • measure only with dosing cup provided
  • do not use dosing cup with other products
  • dose as follows or as directed by a doctor
  • adults and children 12 years of age and older: 20 mL in dosing cup provided every 4 hours
  • children under 12 years of age: do not use

Ingredientes inactivos

anhydrous citric acid, ascorbic acid, edetate disodium, FD&C Blue No. 1, FD&C Red No. 40, flavors, glycerin, propyl gallate, propylene glycol, purified water, sodium benzoate, sodium citrate, sorbitol, sucralose, xanthan gum

¿Preguntas?

1-866-467-2748

— Etiqueta de la FDA de Overnight Cold and Flu, Raritan Pharmaceuticals, vigente desde el 8 de septiembre de 2026. Ver la etiqueta oficial en DailyMed →

Mucinex Nightshift Sinus Maximum Strength · RB Health (US) LLC

Acetaminophen 325 mg · Dextromethorphan hydrobromide 10 mg · Triprolidine hydrochloride 1.25 mg, tableta, recubierta (oral)

Principio activo (in each caplet)

Acetaminophen 325 mg Dextromethorphan HBr 10 mg Triprolidine HCl 1.25 mg

Propósito

Acetaminophen 325 mg ........ Pain reliever/fever reducer Dextromethorphan HBr 10 mg................Cough suppressant Triprolidine HCl 1.25 mg...................................Antihistamine

Usos

  • temporarily relieves these common cold and flu symptoms:
  • cough
  • minor aches and pains
  • sore throat
  • headache
  • runny nose
  • sneezing
  • itching of the nose or throat
  • itchy, watery eyes due to hay fever
  • temporarily reduces fever
  • controls cough to help you get to sleep

Advertencias

  • Liver warning: This product contains acetaminophen. Severe liver damage may occur if you take:
  • more than 8 caplets in 24 hours, which is the maximum daily amount for this product
  • with other drugs containing acetaminophen
  • 3 or more alcoholic drinks daily while using this product
  • Allergy alert: Acetaminophen may cause severe skin reactions. Symptoms may include:
  • skin reddening
  • blisters
  • rash If a skin reaction occurs, stop use and seek medical help right away.
  • Sore throat warning: If sore throat is severe, persists for more than 2 days, is accompanied or followed by fever, headache, rash, nausea, or vomiting, consult a doctor promptly.

Do not use (No use)

  • with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist.
  • if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric, or emotional conditions, or Parkinson’s disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product.

Ask a doctor before use if (Consulte a un médico antes de usar si)

you have

  • liver disease
  • glaucoma
  • trouble urinating due to an enlarged prostate gland
  • a breathing problem such as emphysema or chronic bronchitis
  • persistent or chronic cough such as occurs with smoking, asthma, or emphysema
  • cough that occurs with too much phlegm (mucus)

Ask a doctor or pharmacist before use if (Consulte a un médico o farmacéutico antes de usar si)

you are

  • taking the blood thinning drug warfarin
  • taking sedatives or tranquilizers

When using this product (Al usar este producto)

  • do not use more than directed
  • excitability may occur, especially in children
  • marked drowsiness may occur
  • alcohol, sedatives, and tranquilizers may increase drowsiness
  • avoid alcoholic drinks
  • use caution when driving amotor vehicle or operatingmachinery

Stop use and ask a doctor if (Deje de usarlo y consulte a un médico si)

  • pain or cough gets worse or lasts more than 7 days
  • fever gets worse or lasts more than 3 days
  • redness or swelling is present
  • new symptoms occur
  • cough comes back or occurs with rash or headache that lasts. These could be signs of a serious condition.
  • Overdose warning: Taking more than the recommended dose (overdose) may cause liver damage. In case of overdose, get medical help or contact a Poison Control Center right away. Quick medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.

Keep out of reach of children (Mantener fuera del alcance de los niños)

Instrucciones

  • do not take more than directed (see Overdose warning)
  • do not take more than 8 caplets in any 24-hour period
  • adults and children 12 years of age and over: take 2 caplets every 4 hours
  • children under 12 years of age: do not use

Otra información

  • store at 20-25°C (68-77°F)

Ingredientes inactivos

croscarmellose sodium, crospovidone, hypromellose, microcrystalline cellulose, polyethylene glycol, polysorbate 80, povidone, titanium dioxide

¿Preguntas?

1-866-MUCINEX (1-866-682-4639)

— Etiqueta de la FDA de Mucinex Nightshift Sinus Maximum Strength, RB Health (US) LLC, vigente desde el 15 de mayo de 2025. Ver la etiqueta oficial en DailyMed →

Mucinex Childrens Night Time Multi-Symptom Cold and Flu · Reckitt Benckiser LLC

Acetaminophen 325 mg/10 mL · Dextromethorphan hydrobromide 10 mg/10 mL · Triprolidine hydrochloride 1.25 mg/10 mL, solución (oral)

Principio activo (in each 10 mL)

Acetaminophen 325 mg Dextromethorphan HBr 10 mg Triprolidine HCl 1.25 mg Acetaminophen 325 mg - Pain reliever/fever reducer Dextromethorphan HBr 10 mg - Cough suppressant Triprolidine HCl 1.25 mg.........................Antihistamine

Propósito

Acetaminophen 325 mg - Pain reliever/fever reducer Dextromethorphan HBr 10 mg - Cough suppressant Triprolidine HCl 1.25 mg.........................Antihistamine

Usos

  • temporarily relieves these common cold and flu symptoms:
  • cough
  • minor aches and pains
  • sore throat
  • headache
  • runny nose
  • sneezing
  • itching of the nose or throat
  • itchy, watery eyes due to hay fever
  • temporarily reduces fever
  • controls cough to help your child get to sleep

Advertencias

  • Liver warning: This product contains acetaminophen. Severe liver damage may occur if your child takes:
  • more than 4 doses (40 mL) in 24 hours, which is the maximum daily amount for this product
  • with other drugs containing acetaminophen
  • Allergy alert: Acetaminophen may cause severe skin reactions. Symptoms may include:
  • skin reddening
  • blisters
  • rash If a skin reaction occurs, stop use and seek medical help right away.
  • Sore throat warning: If sore throat is severe, persists for more than 2 days, is accompanied or followed by fever, headache, rash, nausea, or vomiting, consult a doctor promptly.

Do not use (No use)

  • with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist.
  • to make a child sleepy
  • in a child who is taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric, or emotional conditions, or Parkinson’s disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your child’s prescription drug contains an MAOI, ask a doctor or pharmacist before giving this product.

Ask a doctor before use if (Consulte a un médico antes de usar si)

the child has

  • liver disease
  • glaucoma
  • a breathing problem such as chronic bronchitis
  • persistent or chronic cough such as occurs with asthma
  • cough that occurs with too much phlegm (mucus)

Ask a doctor or pharmacist before use if (Consulte a un médico o farmacéutico antes de usar si)

the child is

  • taking the blood thinning drug warfarin
  • taking sedatives or tranquilizers

When using this product (Al usar este producto)

  • do not use more than directed (see Overdose warning)
  • excitability may occur, especially in children
  • marked drowsiness may occur
  • sedatives and tranquilizers may increase drowsiness

Stop use and ask a doctor if (Deje de usarlo y consulte a un médico si)

  • pain or cough gets worse or lasts more than 5 days
  • fever gets worse or lasts more than 3 days
  • redness or swelling is present
  • new symptoms occur
  • cough comes back or occurs with rash or headache that lasts. These could be signs of a serious condition.

Keep out of reach of children (Mantener fuera del alcance de los niños)

Overdose warning : Taking more than the recommended dose (overdose) may cause liver damage. In case of overdose, get medical help or contact a Poison Control Center right away. Quick medical attention is critical for children even if you do not notice any signs or symptoms.

Keep out of reach of children (Mantener fuera del alcance de los niños)

Instrucciones

  • this product does not contain directions or complete warnings for adult use
  • do not give more than directed (see Overdose warning)
  • measure only with dosing cup provided
  • do not use dosing cup with other products
  • dose as follows or as directed by a doctor
  • children 6 to under 12 years of age: 10 mL in dosing cup provided every 4 hours while symptoms last; do not give more than 4 doses in any 24-hour period
  • children under 6 years of age: do not use

Otra información

  • each 10 mL contains: sodium 6 mg
  • store at 20-25ºC (68-77ºF)
  • do not refrigerate

Ingredientes inactivos

ammonium glycyrrhizate, anhydrous citric acid, edetate disodium, FD&C red no. 40, FD&C yellow no. 10, flavors, glycerin (soy), propylene glycol, purified water, sodium benzoate, sorbitol, sucralose, xanthan gum

¿Preguntas?

1-866-MUCINEX (1-866-682-4639)

— Etiqueta de la FDA de Mucinex Childrens Night Time Multi-Symptom Cold and Flu, Reckitt Benckiser LLC, vigente desde el 21 de mayo de 2026. Ver la etiqueta oficial en DailyMed →

Esta página no es un consejo médico. Lea la etiqueta de su envase y pregunte a un farmacéutico o médico si no está seguro de que un medicamento sea adecuado para usted, para su hijo o con sus otros medicamentos.

Mismo medicamento, otras marcas

Cada grupo muestra los productos que tienen exactamente los mismos principios activos, en la misma cantidad y forma, según su registro ante la FDA (directorio NDC). Una marca de tienda del mismo grupo tiene el mismo medicamento que la marca conocida; los ingredientes inactivos, los sabores y el tamaño del envase pueden variar. Cada producto enlaza a su propia etiqueta oficial.

Acetaminophen 650 mg/20 mL · Dextromethorphan hydrobromide 20 mg/20 mL · Triprolidine hydrochloride 2.5 mg/20 mL · solución (oral) · 12 productos

Etiqueta «Drug Facts» de esta concentración y forma ↑

Marca o nombre del productoEmpresa en la etiquetaEtiqueta
Cold and Flu Nighttime Cvs Woonsocket Prescription Center, Incorporated DailyMed
Cold and Flu Nighttime Walgreen Company DailyMed
Cold and Flu Nighttime Walmart Inc. DailyMed
CVS Nighttime Cold and Flu Cvs Health DailyMed
Delsym Nighttime Cough Reckitt Benckiser LLC DailyMed
Meijer Nighttime Cold and Flu Meijer Distribution Inc. —
Mucinex Fast-Max Nighttime Cold and Flu Reckitt Benckiser LLC —
Mucinex Fast-Max Recharge Nighttime Cold and Flu Reckitt Benckiser LLC DailyMed
Mucinex Nightshift Cold and Flu Reckitt Benckiser LLC —
Overnight Cold and Flu Raritan Pharmaceuticals DailyMed
Overnight Cold and Flu Walgreens Co DailyMed
Target Overnight Cold and Flu Target Corporation DailyMed
Acetaminophen 325 mg · Dextromethorphan hydrobromide 10 mg · Triprolidine hydrochloride 1.25 mg · tableta, recubierta (oral) · 3 productos

Etiqueta «Drug Facts» de esta concentración y forma ↑

Marca o nombre del productoEmpresa en la etiquetaEtiqueta
Mucinex Nightshift Cold and Flu Maximum Strength Reckitt Benckiser LLC DailyMed
Mucinex Nightshift Sinus Maximum Strength RB Health (US) LLC DailyMed
Acetaminophen 325 mg/10 mL · Dextromethorphan hydrobromide 10 mg/10 mL · Triprolidine hydrochloride 1.25 mg/10 mL · solución (oral) · 1 producto

Etiqueta «Drug Facts» de esta concentración y forma ↑

Marca o nombre del productoEmpresa en la etiquetaEtiqueta
Mucinex Childrens Night Time Multi-Symptom Cold and Flu Reckitt Benckiser LLC DailyMed

Empresas que venden este medicamento

La empresa que aparece en el envase (fabricante o distribuidor), según el directorio NDC de la FDA, con su número de productos sin receta de este medicamento.

  • Reckitt Benckiser LLC7 productos
  • Walmart Inc.1 producto
  • Walgreens Co1 producto
  • Walgreen Company1 producto
  • Meijer Distribution Inc.1 producto
  • Target Corporation1 producto
  • Cvs Woonsocket Prescription Center, Incorporated1 producto
  • Raritan Pharmaceuticals1 producto
  • Cvs Health1 producto
  • RB Health (US) LLC1 producto

Retiros del mercado

De los informes de la FDA, vinculados por el código NDC o la etiqueta del producto. Un retiro suele afectar a productos o lotes concretos: revise el nombre y el número de lote de su envase.

  1. 15 de abril de 2015 · Clase II · Cerrado por la FDA · D-1369-2015

    Labeling: Label Mix-Up; Bottles of Mucinex Fast-Max liquid are correctly labeled on the front of the label, however the back of the bottle where the Drug Facts labeling is, is missing certain Active Ingredients such as acetaminophen, phenylephrine, dextromethorphan, diphenhydramine, and/or guaifenesin. As a result cert

    Mucinex Fast Max DM Max, Maximum Strength, Dextromethorphan HBr Cough Suppressant, 6 fl oz (180 mL) Bottle, For Ages 12+, Dist. By: Reckitt Benckiser Parsippany, NJ 07054-0224 Made in India, NDC 63824-019-66, UPC 63824-0 — Reckitt Benckiser LLC

Siguientes pasos

Fuentes

  1. Drug labeling (SPL, openFDA) — Administración de Alimentos y Medicamentos de los EE. UU. (FDA), datos de la FDA exportados el 30 de octubre de 2026, consultados el 31 de octubre de 2026
  2. NDC Directory (openFDA) — Administración de Alimentos y Medicamentos de los EE. UU. (FDA), datos de la FDA exportados el 30 de octubre de 2026, consultados el 31 de octubre de 2026
  3. Drug recall enforcement reports (openFDA) — Administración de Alimentos y Medicamentos de los EE. UU. (FDA), datos de la FDA exportados el 27 de octubre de 2026, consultados el 31 de octubre de 2026
  4. Norma de la FDA sobre la etiqueta «Drug Facts» (21 CFR 201.66)

Solo se incluyen medicamentos vendidos según las normas de la FDA para medicamentos sin receta (una monografía o una aprobación de la FDA). No se incluyen productos homeopáticos: la FDA no evalúa su seguridad ni su eficacia.

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