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Over-the-counter medicine · no prescription needed

Menthol and pramoxine

Purpose on the label: Topical anagesic

Other medicines

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 Menthol and pramoxine used for?
The Drug Facts label of CVS Medicated anti itch (Cvs) lists these uses: for the temporary relief of pain and itching due to: minor burns, sunburn, minor cuts, scrapes, insect bites, minor skin irritations ,minor rashes due to poison ivy, poison oak, or poison sumac.
Do I need a prescription for Menthol and pramoxine?
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 Menthol and pramoxine 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.

CVS Medicated anti itch · Cvs

Menthol 1% · Pramoxine hydrochloride 1%, cream (topical)

Active ingredient

Menthol 1% Pramoxine hydrochloride 1%

Purpose

Topical anagesic

Uses

for the temporary relief of pain and itching due to: minor burns, sunburn, minor cuts, scrapes, insect bites, minor skin irritations ,minor rashes due to poison ivy, poison oak, or poison sumac

Warnings

When using this product

do not get into eyes

Keep out of reach of children

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

Directions

Adults and Children 2 years and older: Apply to affected are not more than 3 to 4 times daily.

Inactive ingredients

aloe barbadensis (aloe vera) leaf juice, diazolidinyl urea, edetate disodium, eucalyptus oil, methylparaben, methyl salicylate, propylene glycol, propylparaben, purified water, sodium polyacrylate, steareth-21, stearyl alcohol, tocopheryl acetate, trolamine, white petrolatum

— FDA label of CVS Medicated anti itch, Cvs, effective December 12, 2023. See the official label on DailyMed →

Gold Bond Intensive Relief Anti-Itch · Chattem, Inc.

Menthol 0.5% · Pramoxine hydrochloride 1%, lotion (topical)

Active ingredient

Menthol 0.5% Pramoxine hydrochloride 1%

Purpose

Anti-itch Anti-itch

Uses

for temporary relief of pain and itching associated with:

  • minor burns
  • sunburn
  • minor cuts
  • scrapes
  • insect bites
  • minor skin irritations

Warnings

For external use only

When using this product

  • avoid contact with eyes

Stop use and ask a doctor if

  • condition worsens
  • symptoms persist for more than 7 days or 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 immediately.

Directions

adults and children 2 years of age and older : apply freely to affected area not more than 3 to 4 times daily children under 2 years of age : consult a doctor

Inactive ingredients

water, glycerin, dimethicone, cetyl alcohol, petrolatum, distearyldimonium chloride, aloe barbadensis leaf juice, glyceryl stearate, stearyl alcohol, cetearyl alcohol, behentrimonium methosulfate, steareth-21, propylene glycol, polysorbate 60, stearamidopropyl PG-dimonium chloride phosphate, diazolidinyl urea, butylene glycol, tocopheryl acetate, potassium hydroxide, methylparaben, panthenol, ethoxydiglycol, EDTA, avena sativa (oat) kernel extract

— FDA label of Gold Bond Intensive Relief Anti-Itch, Chattem, Inc., effective January 14, 2026. See the official label on DailyMed →

Sarna · Crown Laboratories, Inc

Menthol 0.5 mg/1000 mL · Pramoxine hydrochloride 10 mg/1000 mL, lotion (topical)

Active ingredient

Menthol 0.5% Pramoxine Hydrochloride 1%

Purpose

External analgesic

Uses

for the temporary relief of pain and itching associated with minor burns, sunburn, minor cuts, scrapes, insect bites, minor skin irritations and rashes due to poison ivy, poison oak, or poison sumac

Warnings

For external use only.

Do not use

in the eyes or nose over large areas of the body for prolonged periods

When using this product

avoid contact with the eyes. if condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and consult a doctor.

Stop use and ask a doctor if

redness, irritation, swelling, or pain persists or increases.

Keep out of reach of children

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

Directions

to open, hold cap and turn pump clockwise. Adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times daily. Children under 2 years of age: do not use, consult a doctor.

Inactive ingredients

Aloe Barbadensis Leaf Juice, Benzyl Alcohol, Beta-Glucan, Butylene Glycol, C12-18 Alkanoyl Glycerin/Sebacic Acid Copolymer, Caprylyl Glycol, Carbomer, Cetyl Alcohol, Dimethicone, Ethylhexylglycerin, Glycerin, Glyceryl Stearate, Hamamelis Virginiana (Witch Hazel) Leaf Extract, Isopropyl Myristate, Palmitic Acid, PEG-100 Stearate, PEG-8 Stearate, Pentylene Glycol, Sodium Hydroxide, Stearic Acid, Tocopherol, Water

Questions?

call 1-833-279-6522

— FDA label of Sarna, Crown Laboratories, Inc, effective January 12, 2026. See the official label on DailyMed →

Terramed Just Think Comfort HerpCare EXTERNAL ANALGESIC FOR THE TEMPORARY RELIEF OF ITCHING AND IRRITATION · Rida LLC

Menthol 0.1% · Pramoxine hydrochloride 1%, ointment (topical)

Active ingredient (in each gram)

Purpose Menthol 0.1%......................................................................External analgesic Pramoxine hydrochloride 1%..................................................External analgesic

Uses

temporarily relieves itching and irritation of the external genital area associated with minor skin irritation

Warnings

For external use only.

Do not use

in or around the eyes internally

When using this product

use only as directed avoid contact with the eyes and mucous membranes do not apply to open wounds or broken skin

Stop use and ask a doctor if

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

If pregnant or breast-feeding

ask a health professional before use.

Keep out of reach of children

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

Directions

adults and children 12 years of age and older: apply to the affected area not more than 3 to 4 times daily children under 12 years of age: ask a doctor

Inactive ingredients

alcohol, bee propolis extract, beeswax, calendula officinalis extract, castor oil, colloidal oatmeal, glycerin, lemongrass oil, melissa officinalis (lemon balm) oil, olive extract, olive oil (oxygenated), symphytum officinale (comfrey) extract, willow bark extract.

— FDA label of Terramed Just Think Comfort HerpCare EXTERNAL ANALGESIC FOR THE TEMPORARY RELIEF OF ITCHING AND IRRITATION, Rida LLC, effective June 23, 2026. See the official label on DailyMed →

Anti Itch Maximum Relief · Natureplex LLC

Menthol, unspecified form 1% · Pramoxine hydrochloride 1%, cream (topical)

Active ingredient

Purpose Menthol 1% Topical Analgesic Pramoxine hydrochloride 1% Topical Analgesic

Purpose

Active ingredients Purpose Menthol 1% Topical Analgesic Pramoxine hydrochloride 1% Topical Analgesic

Uses

For temporary relief of pain and itching associated with minor skin irritations, minor burns, minor cuts, sunburns, scrapes, insect bites, and rashes due to poison ivy, poison oak, or poison sumac

Warnings

For external use only. Avoid contact with eyes and nose. Not for prolonged use.

Do not use

on large areas of the body

Stop use and ask a doctor if

condition worsens symptoms persist for more than 7 days or clear up and occur again within a few days redness, irritation, swelling, or pain develops, persists, or increases

If pregnant or breast-feeding

ask a health professional before use.

Keep out of reach of children

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

Directions

adults and children 2 years old and older: apply to affected area not more than 3 to 4 times daily children under 2 years old: ask a doctor

Inactive ingredients

aloe barbadensis leaf juice, carbomer, cetearyl alcohol, DMDM hydantoin, glycerin, polysorbate 60, propylene glycol, purified water, triethanolamine

Questions?

866-323-0107 or www.natureplex.com

— FDA label of Anti Itch Maximum Relief, Natureplex LLC, effective August 28, 2025. 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.

Menthol 1% · Pramoxine hydrochloride 1% · cream (topical) · 5 products

Drug Facts for this strength and form ↑

Brand or product nameCompany on the labelLabel
Best Choice Medicated anti itch Value Merchandisers DailyMed
CVS Medicated anti itch Cvs DailyMed
Family Care Maximum Strength Medicated Anti Itch United Exchange Corp. DailyMed
Freds Medicated anti itch Discount Drug Mart DailyMed
QC Medicated anti itch Chain Drug Marketing Association DailyMed
Menthol 0.5% · Pramoxine hydrochloride 1% · lotion (topical) · 2 products

Drug Facts for this strength and form ↑

Brand or product nameCompany on the labelLabel
Gold Bond Intensive Relief Anti-Itch Chattem, Inc. DailyMed
Gold Bond Medicated Anti-Itch Gold Bond Co LLC DailyMed
Menthol 0.5 mg/1000 mL · Pramoxine hydrochloride 10 mg/1000 mL · lotion (topical) · 1 product

Drug Facts for this strength and form ↑

Brand or product nameCompany on the labelLabel
Sarna Crown Laboratories, Inc DailyMed
Menthol 0.1% · Pramoxine hydrochloride 1% · ointment (topical) · 1 product

Drug Facts for this strength and form ↑

Brand or product nameCompany on the labelLabel
Terramed Just Think Comfort HerpCare EXTERNAL ANALGESIC FOR THE TEMPORARY RELIEF OF ITCHING AND IRRITATION Rida LLC DailyMed
Menthol, unspecified form 1% · Pramoxine hydrochloride 1% · cream (topical) · 1 product

Drug Facts for this strength and form ↑

Brand or product nameCompany on the labelLabel
Anti Itch Maximum Relief Natureplex 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.

  • Chattem, Inc.1 product
  • Crown Laboratories, Inc1 product
  • Rida LLC1 product
  • Chain Drug Marketing Association1 product
  • Cvs1 product
  • Gold Bond Co LLC1 product
  • Discount Drug Mart1 product
  • United Exchange Corp.1 product
  • Value Merchandisers1 product
  • Natureplex LLC1 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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