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Over-the-counter medicine · no prescription needed

Benzalkonium and benzocaine

Purpose on the label: First Aid Antiseptic Topical Pain Relief

Pain relief on the skin

Official FDA data, not advice

The label text is quoted exactly as the company filed it with the U.S. Food and Drug Administration (FDA), with a link to the official copy. The list of brands comes from the FDA NDC Directory.

This page is not medical advice. Read the label on your package, and ask a pharmacist or doctor if you are not sure a medicine is right for you, for your child, or with your other medicines.

If someone may have taken too much, call Poison Help: 1‑800‑222‑1222. In an emergency, call 911.

Quick answers

What is Benzalkonium and benzocaine used for?
The Drug Facts label of First Aid Only Antiseptic First Aid (Acme United Corporation) lists these uses: First Aid to help prevent infection and for temporary pain relief in minor cuts, scrapes, burns. clean affected area spray over the area 1 to 3 times daily may be covered with a sterile bandage (let it dry first) children under 2 ask a doctor.
Do I need a prescription for Benzalkonium and benzocaine?
No. The products on this page are sold without a prescription (over the counter).
Is a store brand the same as the name brand?
Products listed together below have the same active ingredients, in the same amount and the same form, as registered with the FDA. Inactive ingredients (such as colors, flavors and fillers) and package sizes can differ. Compare the “Active ingredient” box on both packages, and ask a pharmacist if you are not sure.
Has Benzalkonium and benzocaine been recalled?
No recall linked to these products appears in the FDA enforcement reports we use.

Drug Facts label

Every over-the-counter medicine must carry a “Drug Facts” box in the same order, set by FDA rules. Below is the label of one product for each common strength and form, quoted word for word. Your own package can differ (for example, children’s products have other directions): always follow the label on your package.

First Aid Only Antiseptic First Aid · Acme United Corporation

Benzalkonium chloride 0.1% · Benzocaine 5%, spray (topical)

Active ingredient

Benzalkonium Chloride 0.1% Purpose First Aid Antiseptic Benzocaine 5.0% Purpose Topical Pain Relief

Purpose

Drug Facts Benzalkonium Chloride 0.1% Purpose First Aid Antiseptic Benzocaine 5.0% Purpose Topical Pain Relief

Uses

First Aid to help prevent infection and for temporary pain relief in minor cuts, scrapes, burns. clean affected area spray over the area 1 to 3 times daily may be covered with a sterile bandage (let it dry first) children under 2 ask a doctor

Warnings

For External use Only Flammable. Keep away from fire or flame Do Not Use

  • near eyes or mucous membranes
  • on deep or puncture wounds, animal bites, or serious burns
  • Over large areas of the body
  • More than one week unless directed by a doctor.

Stop use and ask a doctor if

condition persists or gets worse Keep out of the reach of children If swallowed, get medical help or contact Poison Control Center right away

Directions

clean affected area spray over the area 1 to 3 times daily may be covered with a sterile bandage (let it dry first) children under 2 ask a doctor

Inactive ingredients

isopropyl alcohol, purified water

Questions?

1.800.835.2263

— FDA label of First Aid Only Antiseptic First Aid, Acme United Corporation, effective May 23, 2025. See the official label on DailyMed →

American Red Cross Antiseptic · My Imports USA LLC

Benzalkonium chloride 0.13% · Benzocaine 5%, spray (topical)

Active ingredient

Benzalkonium Chloride 0.13%(w/w) Benzocaine 5.00%(w/w)

Purpose

First Aid Antiseptic Topical Analgesic

Uses

temporarily relieves pain and itching due to: subburn, minor burns, minor cuts, scrapes, insect bite, minor skin irritations

Warnings

For external use only. Flammable, keep away from heat, spark, electrical, fire or flame.

Do not use

  • Allergy alert: do not use this product if you have a history or allergy to local anesthetics such as procaine, butacaine, benzocaine or other "caine" anesthetics.

When using this product

When using this product

avoid contact with eyes use only as directed. Intentional misuse by deliberately concentrating and inhaling can be harmful or fatal. contents under pressure. Do not puncture or incinerate. Do not store at temperature above 120ºF.

Stop use and ask a doctor if

Stop use and ask a doctor if

condition worsens symptoms last more than 7 days or clear up and occur again with a few days itching, rash or irritation develops

Keep out of reach of children

If product is swallowed, get medical help or contact a Poison Control Center right away.

Directions

adult and children 2 years or older: apply to affected area not more than 3 to 4 times daily. children under 2 years of age: ask a doctor to use this product, hold the can 6 to 12 inches away from the affected area. Direct apray nozzles towards skin and press the button to activate spray to apply to face, spray into palm of hand and gently apply.

Inactive ingredients

Propane Ethyl alcohol Butane Glycerin Propylene glycol

— FDA label of American Red Cross Antiseptic, My Imports USA LLC, effective October 27, 2025. See the official label on DailyMed →

Quality Choice Oral Pain Relief · Quality Choice (CHAIN DRUG MARKETING ASSOCIATION)

Benzalkonium chloride 1% · Benzocaine 20%, gel (topical)

Active ingredient

Benzocaine 20% Benzalkonium Chloride 0.1%

Purpose

Oral pain reliever Antiseptic

Uses

for the temporary relief of pain due to toothaches to help protect against infection in minor oral irritation

Warnings

Methemoglobinemia warning : use of this product may cause methemoglobinemia, a serious condition that must be treated promptly because it reduces the amount of oxygen carried in blood. This can occur even if you have used this product before. Stop use and seek immediate medical attention if you or a child in your care develops:

  • pale, gray or blue-colored skin (cyanosis)
  • headache
  • rapid heart rate
  • shortness of breath
  • dizziness or lightheadedness
  • fatigue or lack of energy
  • Allergy alert: do not use this product if you have a history of allergy to local anesthetics such as procaine, butacaine, benzocaine, or other "caine" anesthetics

Do not use

more than directed for more than 7 days unless directed by a physician or healthcare provider for teething in children under 2 years of age Stop use and ask a physician if swelling, rash or fever develops irritation, pain or redness persists or worsens symptoms do not improve in 7 days KEEP OUT OF REACH OF CHILDREN: In case of overdose or allergic reaction, get medical help or contact a Poison Control Center right away (1-800-222-1222)

Directions

Adults and children 2 years of age and over - Apply a small amount of product to the cavity and around the gum surrounding the teeth. Use up to 4 times daily or as directed by a physician or healthcare provider Children under 12 years of age - Should be supervised in the use of this product Children under 2 years of age -do not use

Other information

this preparation is intended for use in cases of toothache, only as a temporary expedient until a physician can be consulted do not use continuously avoid using toothpaste or drinking soft drinks or fruit juices for at least one hour after applying do not use if tube seal under cap is broken store at 20-25C (68-77F)

Inactive ingredients

glycerin, PEG 400, propylene glycol, sorbitol, sodium saccharine, sorbic acid, sodium polyacrylate,strawberry flavor, water

Questions?

TOLL FREE 800-935-2362

— FDA label of Quality Choice Oral Pain Relief, Quality Choice (CHAIN DRUG MARKETING ASSOCIATION), effective April 15, 2024. See the official label on DailyMed →

First Aid · HART Health

Benzalkonium chloride 0.001 mg/mg · Benzocaine 0.05 mg/mg, spray (topical)

Active ingredient

Benzalkonium Chloride 0.1% Benzocaine 5.0%

Purpose

Topical Antiseptic Topical Anethetic

Uses

First aid to help protect against skin infection and for the temporary relief of pain and itching in minor cuts and scrapes bites skin irritation

Warnings

For external use only. Flammable, keep away from heat or flame

Do not use

in or near the eyes over large portions of the body in large quantities, particularly over raw surfaces or blistered areas on deep or puncture wounds on animal bites on serious burns longer than 7 days unless directed by a doctor

Stop use and ask a doctor if

condition worsens symptoms persist for more than 7 days symptoms clear up and occur again within a few days

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away. 1-800-222-1222

Directions

clean affected area and spray 1 to 3 times daily may be covered with a sterile bandage Children under 2 years of age: ask a doctor

Inactive ingredients

Isopropyl Alcohol, Purified Water

— FDA label of First Aid, HART Health, effective January 18, 2024. See the official label on DailyMed →

DEBACHERE Butt Balm After Care Antiseptic Pain Relief · De.Bachere USA LLC

Benzalkonium chloride 1 mg/mL · Benzocaine 50 mg/mL, cream (topical)

Active ingredient

Benzocaine 5.00% Benzalkonium Chloride 0.10% Purpose Topical Analgesic Antiseptic

Purpose

Topical Analgesic Antiseptic

Uses

For the temporary relief of pain associated with burns, sunburn, minor cuts, scrapes, insect bites, and minor skin irritations. First aid help prevent infection in minor cuts, scrapes, and burns.

Warnings

For external use only, not intended for ingestion.

Do not use

in the eyes or apply over large areas of the body. In case of deep or puncture wounds, animal bites, or serious burns, consult a doctor.

When using this product

avoid contact with the eyes.

Stop use and ask a doctor if

The condition persists or gets worse.

Do not use

longer than 1 week unless directed by a doctor.

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away.

If pregnant or breast-feeding

ask a health professional before use.

Directions

Clean the affected area. Adults and children 2 years of age and older. Apply to the affected area not more than 3 to 4 times daily. Children under 2 years of age: Consult a doctor.

Inactive ingredients

Inactive Ingridients: Aloe extract, Beeswax, Camphor, Cetyl Esters, Ethyl vanillin, Helianthus (sunflower) Oil, Lanolin, Menthol, Paraffin Wax, Salicylic Acid, Theobroma Cacao (cocoa) butter, FD&C Blue # 1.

— FDA label of DEBACHERE Butt Balm After Care Antiseptic Pain Relief, De.Bachere USA LLC, effective October 29, 2024. See the official label on DailyMed →

Oral Gel Oral Pain Relief · Savvy Care and Cosmetics

Benzalkonium chloride 0.1% · Benzocaine 20%, gel (topical)

Active ingredient

Benzocaine 20% Benzalkonium Chloride 0.1%

Purpose

Oral pain reliever Antiseptic

Uses

  • for the temporary relief of pain due to toothaches
  • to help protect against infectionin minor oral irritation

Warnings

  • Allergy alert: do not use this product if you have a history of allergy to local anesthetics such as procaine, butacaine or other "caine" anesthetics

Do not use

  • more than directed
  • for more than 7 days unless directed by a physician or healthcare provider Stop use and ask a physician if
  • swelling, rash or fever develops
  • irritation, pain or redness persists or worsens
  • symptoms do not improve in 7 days

Keep out of reach of children

In case of overdose or allergic reaction get medical help or contact a Poison Control Center right away

Directions

  • adults and children 2 years of age and over: apply a small amount of the product to the cavity and around the gum surrounding the teeth Use up to 4 times daily or as directed by a physician or healthcare provider
  • children under 12 years: should be supervised in the use of this product
  • children under 2 years of age: ask a physician or health care provider

Inactive ingredients

ammonium glycyrrhizate, flavor, polyethylene glycol, sodium saccharin, sorbic acid

— FDA label of Oral Gel Oral Pain Relief, Savvy Care and Cosmetics, effective December 19, 2024. See the official label on DailyMed →

This page is not medical advice. Read the label on your package, and ask a pharmacist or doctor if you are not sure a medicine is right for you, for your child, or with your other medicines.

Same medicine, other brands

Each group lists the products that have exactly the same active ingredients, in the same amount and form, as registered with the FDA (NDC Directory). A store brand in the same group has the same medicine as the name brand; inactive ingredients, flavors and package sizes can differ. Each product links to its own official label.

Benzalkonium chloride 0.1% · Benzocaine 5% · spray (topical) · 3 products

Drug Facts for this strength and form ↑

Brand or product nameCompany on the labelLabel
Antiseptic Safetec of America, Inc. DailyMed
Antiseptic Wildman Business Group DailyMed
First Aid Only Antiseptic First Aid Acme United Corporation DailyMed
Benzalkonium chloride 0.13% · Benzocaine 5% · spray (topical) · 2 products

Drug Facts for this strength and form ↑

Brand or product nameCompany on the labelLabel
American Red Cross Antiseptic My Imports USA LLC DailyMed
American Red Cross Antiseptic Zhejiang Guoyao Jingyue Aerosol Co., Ltd. DailyMed
Benzalkonium chloride 1% · Benzocaine 20% · gel (topical) · 2 products

Drug Facts for this strength and form ↑

Brand or product nameCompany on the labelLabel
Oral Pain Relief Universal Distribution Center LLC —
Quality Choice Oral Pain Relief Quality Choice (CHAIN DRUG MARKETING ASSOCIATION) DailyMed
Benzalkonium chloride 0.001 mg/mg · Benzocaine 0.05 mg/mg · spray (topical) · 1 product

Drug Facts for this strength and form ↑

Brand or product nameCompany on the labelLabel
First Aid HART Health DailyMed
Benzalkonium chloride 1 mg/mL · Benzocaine 50 mg/mL · cream (topical) · 1 product

Drug Facts for this strength and form ↑

Brand or product nameCompany on the labelLabel
DEBACHERE Butt Balm After Care Antiseptic Pain Relief De.Bachere USA LLC DailyMed
Benzalkonium chloride 0.1% · Benzocaine 20% · gel (topical) · 1 product

Drug Facts for this strength and form ↑

Brand or product nameCompany on the labelLabel
Oral Gel Oral Pain Relief Savvy Care and Cosmetics DailyMed
Benzalkonium chloride 0.1% · Benzocaine 4% · solution (topical) · 1 product
Brand or product nameCompany on the labelLabel
Hug a BooBoo Medicated booboo Wipes Lights Medical Manufacture Co., Ltd. DailyMed
Benzalkonium chloride 100 mg/mL · Benzocaine 50 mg/mL · spray (topical) · 1 product
Brand or product nameCompany on the labelLabel
Antiseptic JHK Inc DailyMed
Benzalkonium chloride 1.3 mg/mL · Benzocaine 50 mg/mL · liquid (topical) · 1 product
Brand or product nameCompany on the labelLabel
Orajel Cold Sore Touch Free - Single Dose Church & Dwight Co., Inc. DailyMed
Benzalkonium chloride 0.13% · Benzocaine 5% · cream (topical) · 1 product
Brand or product nameCompany on the labelLabel
CVS Pharmacy Sensitive Medicated Cream CVS Pharmacy DailyMed
Benzalkonium chloride 10 mg/mL · Benzocaine 50 mg/mL · cream (topical) · 1 product
Brand or product nameCompany on the labelLabel
DEBACHERE Butt Balm After Play Care Multi Symptoms Relief De.Bachere USA LLC DailyMed

Companies that sell this medicine

The company named on the package (maker or distributor), as listed in the FDA NDC Directory, with its number of over-the-counter products of this medicine.

  • De.Bachere USA LLC2 products
  • Safetec of America, Inc.1 product
  • HART Health1 product
  • My Imports USA LLC1 product
  • Savvy Care and Cosmetics1 product
  • Wildman Business Group1 product
  • Acme United Corporation1 product
  • Universal Distribution Center LLC1 product
  • Lights Medical Manufacture Co., Ltd.1 product
  • JHK Inc1 product
  • Quality Choice (CHAIN DRUG MARKETING ASSOCIATION)1 product
  • Church & Dwight Co., Inc.1 product
  • CVS Pharmacy1 product
  • Zhejiang Guoyao Jingyue Aerosol Co., Ltd.1 product

Recalls

No recall linked to these products (by their NDC code or label) appears in the FDA enforcement reports.

Sources

  1. Drug labeling (SPL, openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  2. NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  3. Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
  4. FDA rule for the Drug Facts label (21 CFR 201.66)

Only medicines marketed under FDA rules for nonprescription drugs (an FDA monograph or an FDA approval) are listed. Homeopathic products are not listed: the FDA does not evaluate them for safety or effectiveness.

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