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Over-the-counter medicine · no prescription needed

Benzalkonium and pramoxine

Purpose on the label: First aid antiseptic Topical analgesic

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 pramoxine used for?
The Drug Facts label of Band Aid Antiseptic Cleansing (Kenvue Brands LLC) lists these uses: Uses first aid to help prevent infection and temporarily relieve pain or discomfort in minor; cuts; scrapes; burns.
Do I need a prescription for Benzalkonium 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 Benzalkonium 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.

Band Aid Antiseptic Cleansing · Kenvue Brands LLC

Benzalkonium chloride 1.3 mg/mL · Pramoxine hydrochloride 10 mg/mL, spray (topical)

Active ingredient

Benzalkonium Cl (0.13%) Pramoxine HCl (1.0%)

Purpose

First aid antiseptic Topical analgesic

Uses

Uses first aid to help prevent infection and temporarily relieve pain or discomfort in minor:

  • cuts
  • scrapes
  • burns

Warnings

For external use only.

Do not use

· in the eyes

  • over large areas of the body

Ask a doctor before use if

you have deep or puncture wounds · animal bites serious burns

Stop use and ask a doctor if

condition or symptoms get worse or last more than 1 week 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.

Directions

adults and children 2 years of age and older: clean the affected area spray a small amount of this product on the area 1 to 3 times daily may be covered with a sterile bandage if bandaged, let dry first children under 2 years of age: consult a doctor

Inactive ingredients

Water, Propylene Glycol, Disodium EDTA

Questions?

call 800-526-3967 or 215-273-8755 (collect).

— FDA label of Band Aid Antiseptic Cleansing, Kenvue Brands LLC, effective June 5, 2025. See the official label on DailyMed →

Maximum Strength Betadine Clear · Atlantis Consumer Healthcare, Inc.

Benzalkonium chloride 0.13 mg/mL · Pramoxine hydrochloride 1 mg/mL, spray (topical)

Active ingredient

Drug Facts Active ingredients Benzalkonium Cl 0.13% Pramoxine HCl 1.0%

Purpose

First aid Antiseptic Topical analgesic

Uses

First aid to help prevent infection and relieve pain or discomfort in minor

  • cuts
  • scrapes
  • burns

Warnings

For external use only

Do not use

  • in the eyes
  • over large areas of the body

Ask a doctor before use if

you have

  • deep or puncture wounds
  • serious burns
  • animal bites

Stop use and ask a doctor if

  • condition or symptoms get worse or last more than 1 week
  • 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 at 1-800-222-1222.

Directions

  • adults and children 2 years of age and older:
  • clean the affected area
  • spray a small amount of this product on the area 1 to 3 times daily
  • may be covered with sterile bandage
  • if bandaged, let dry first
  • children under 2 years of age:
  • consult a doctor

Inactive ingredients

citric acid anhydrous, disodium edetate, flavor, propylene glycol, purified water, sodium citrate dihydrate.

— FDA label of Maximum Strength Betadine Clear, Atlantis Consumer Healthcare, Inc., effective August 31, 2026. See the official label on DailyMed →

T.N. Dickinsons Wound Cleansing · Dickinson Brands Inc.

Benzalkonium chloride 0.0013 g/mL · Pramoxine hydrochloride 0.01 g/mL, liquid (topical)

Active ingredient

Purposes Benzalkonium Chloride (0.13%) First aid antiseptic Pramoxine Hydrochloride (1.0%) Topical analgesic

Purpose

Active ingredients Purposes Benzalkonium Chloride (0.13%) First aid antiseptic Pramoxine Hydrochloride (1.0%) Topical analgesic

Uses

First aid to help prevent infection and temporarily relieve pain or discomfort in minor: cuts scrapes insect bites burns sunburn skin irritations

Warnings

For external use only

Do not use

in the eyes over large areas of the body

Ask a doctor before use if

you have deep or puncture wounds animal bites serious burns Stop use and ask doctor if condition or symptoms get worse or lasts more than 1 week symptoms clear up and occur again within a few days

Keep out of reach of children

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

Directions

adults and children 2 years of age and older: clean the affected area spray a small amount of this product on the area 1 to 3 times daily may be covered with a sterile bandage if bandaged, let dry first children under 2 years of age: consult a doctor

Inactive ingredients

aloe barbadensis leaf juice, benzoic acid, hamamelis virginiana distillate, propanediol, tocopheryl acetate (vitamin E)

Questions?

TNDickinsons.com 1•888•860•2279

— FDA label of T.N. Dickinsons Wound Cleansing, Dickinson Brands Inc., effective December 1, 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.

Benzalkonium chloride 1.3 mg/mL · Pramoxine hydrochloride 10 mg/mL · spray (topical) · 2 products

Drug Facts for this strength and form ↑

Brand or product nameCompany on the labelLabel
Band Aid Antiseptic Cleansing Kenvue Brands LLC DailyMed
Band Aid Antiseptic Cleansing To Go Kenvue Brands LLC DailyMed
Benzalkonium chloride 0.13 mg/mL · Pramoxine hydrochloride 1 mg/mL · spray (topical) · 1 product

Drug Facts for this strength and form ↑

Brand or product nameCompany on the labelLabel
Maximum Strength Betadine Clear Atlantis Consumer Healthcare, Inc. DailyMed
Benzalkonium chloride 0.0013 g/mL · Pramoxine hydrochloride 0.01 g/mL · liquid (topical) · 1 product

Drug Facts for this strength and form ↑

Brand or product nameCompany on the labelLabel
T.N. Dickinsons Wound Cleansing Dickinson Brands Inc. 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.

  • Kenvue Brands LLC2 products
  • Atlantis Consumer Healthcare, Inc.1 product
  • Dickinson Brands Inc.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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