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Over-the-counter medicine · no prescription needed

Benzethonium and lidocaine

Purpose on the label: Topical Antiseptic Topical Anesthetic

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 Benzethonium and lidocaine used for?
The Drug Facts label of Blood Clotting (HART Health) lists these uses: for help in control of superficial bleeding for the temporary relief of paid to help protect against skin infection in minor cuts, scrapes, and burns.
Do I need a prescription for Benzethonium and lidocaine?
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 Benzethonium and lidocaine 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.

Blood Clotting · HART Health

Benzethonium chloride 170 mg/85 g · Lidocaine 3400 mg/85 g, aerosol, spray (topical)

Active ingredient

Benzethonium Chloride 0.2% w/w Lidocaine 4% w/w

Purpose

Topical Antiseptic Topical Anesthetic

Uses

for help in control of superficial bleeding for the temporary relief of paid to help protect against skin infection in minor cuts, scrapes, and burns

Warnings

For external use only Flammable keep away from flame contents under pressure do not puncture or incinerate container do not expose to temperatures above 120°F

Do not use

in or near the eyes or other mucus membranes over large portions of the body on deep or puncture wounds, raw surfaces, blistered areas, animal bites, or serious burns Stop use and ask doctor if redness, swelling, or irritation occurs infection occurs condition persists or worsens symptoms persist for more than 7 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

Adults and children 23 years of age and over: shake can well before using hold 6-8 inches from moist injured area spray until area is covered and superficial bleeding is stopped repeat as necessary scab-like cover will gradually disappear as healing takes place or may be removed with soap and water Children under 12 years of age: ask a doctor

Other information

avoid inhaling use only as directed intentional misuse by deliberately concentrating and inhaling the contents may be harmful or fatal

Inactive ingredients

isobutane, isopropyl myristate, karaya, n-butane, propane, silica, sorbitan monooleate, talc, tragacanth

— FDA label of Blood Clotting, HART Health, effective January 14, 2026. See the official label on DailyMed →

Forticept Wounds and Burns Hydrogel · Lidan, Inc.

Benzethonium chloride 0.001 kg/kg · Lidocaine 0.04 kg/kg, gel (topical)

Active ingredient

DRUG FACTS Active Ingredient/Purpose: LIDOCAINE HCL (4.0%)..........................Topical Analgesic BENZETHONIUM CHLORIDE (0.1%)....................Antiseptic

Purpose

Uses: For temporary relief of pain or discomfort for superficial and full thickness burns or wounds. Topical antiseptic to help decrease the risk of infections. Helps protect skin and supports healing of cuts, scrapes, burns, and wounds.

Uses

Topical analgesic - for temporary relief of pain or discomfort for superficial and full thickness burns or wounds. Topical antiseptic - to help decrease the risk of wounf and skin infections.

Warnings

For external use only!

Do not use

on children under 2 years of age unless directed by a doctor. For children under 2 years of age: please, consult a doctor

When using this product

avoid contact with eyes. Discontinue Use after 7 days unless directed by a doctor

Keep out of reach of children

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

Directions

Adults and children 2 years of age and older:

  • Clean affected area from dirt and debris, let it dry.
  • Apply Forticept Analgesic Antiseptic Hydrogel and cover affected area with a clean gauze if needed.
  • Repeat this procedure 1-3 times daily or as needed until condition improves or medical assistance is rendered.

Inactive ingredients

ALLANTOIN, ALPHA TOCOPHEROL, C13-14 ISOPARAFFIN, CETOSTEARYL ALCOHOL, CHLORPHENESIN, D-PANTHENOL, FD&C BLUE #1, GLYCERIN, HYDROLYZED COLLAGEN, LANOLIN, LAURETH-7, PARAFFINUM LIQUIDUM, PETROLATUM, POLYACRYLAMIDE, POLYHEXANIDE, SHEA BUTTER, STEARETH-2, STEARETH-21, THYMOL, WATER

Questions?

For Questions: Lidan, Inc. 30 Wall Street, 8th Floor New York, NY 10005 www.forticept.com Please call: +1 212 709-8133

— FDA label of Forticept Wounds and Burns Hydrogel, Lidan, Inc., effective March 25, 2025. See the official label on DailyMed →

Super-Stop BloodClotter · Cintas Corp

Benzethonium chloride 0.2 mg/100 mg · Lidocaine 4 mg/100 mg, aerosol, spray (topical)

Active ingredient

Benzethonium Chloride 0.2% w/w Lidocaine 4% w/w

Purpose

Topical Antiseptic Topical Anesthetic

Uses

for help in control of superficial bleeding for temporary relief of pain and to help protect against infection in minor cuts minor scrapes minor burns

Warnings

For external use only Flammable keep away from fire or flame

Do not use

in or near eyes or other mucus membranes on large portion of the body in case of deep or puncture wounds on raw surfaces on blistered areas on animal bites on serious burns

When using this product

avoid spraying in eyes contents under pressure do not puncture or incinerate do not store at temperatures above 120°F use only as directed intentional misuse by deliberately concentrating and inhaling the contents can be harmful or fatal

Stop use and ask a doctor if

redness, swelling, or irritation occurs infection occurs condition worsens or symptoms persist for more than 7 days

Keep out of reach of children

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

Directions

shake can well before using hold 6-8 inches from moist injured area spray until area is covered scab-like cover will gradually disappear as healing takes place or may be removed with soap and water for adult institutional use only not intended for use on children

Inactive ingredients

Isobutane, Isopropyl Myristate, Karaya, N-Butane, Propane, Silica, Sorbitan Monooleate, Talc, and Tragacanth

— FDA label of Super-Stop BloodClotter, Cintas Corp, effective September 26, 2025. See the official label on DailyMed →

Dr. Numb · Shinpharma Inc

Benzethonium chloride 0.25 mg/50 g · Lidocaine 4 mg/50 g, cream (topical)

Active ingredient

Lidocaine 4% benzethonium Chloride 0.25%

Purpose

External Analgesic and First Aid Antiseptic

Uses

Can be used instead of soap and water to help clean minor cuts, scrapes, and burns For the temporary relief of discomfort and pain associated with dermal procedures such as tattoo removal, dermarolling, electrolysis, microblading, and piercing Temporarily relieves pain and itch while helping to prevent infection.

Warnings

For external use only avoid contact with eyes ​​

Do not use

do not use in large quantities particularly over raw surfaces or blistered area do not exceed the recommended dosage unless directed by a doctor in the eyes or apply over large areas of body longer than one week unless directed by a doctor

Ask a doctor before use if

you have deep or puncture wounds, animal bites or serious burns Stop the use and consult doctor if: condition worsenss or symptoms persist for more than 7 days or clear up and occur again within few days.

Keep out of reach of children

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

Directions

Use Dr.Numb® Topical Anesthetic Foam Soap to cleanse the targeted area. Shake well before each use. Apply 2 to 3 pumps of foam soap andgently rub into the skin. Leave it onfor 5 to 10 minutes. Rinse off gentlywith running water or wipe with cleanpaper towel. Use before, during andafter the procedure. Make sure tocover the bottle tightly when not inuse, otherwise, the anesthetic effect will be lessened. Adults and children two years old and older: Use to clean minor cuts, scrapes, and burns by thoroughly washing with water. Rinse and air dry. Use no more than three times daily. Children under two years of age, ask a doctor.

Inactive ingredients

Allantoin, Aloe Barbadensis Leaf Juice, Arnica Montana Flower Extract, Benzyl Alcohol, Glycerin , Lauramidopropyl Betaine, Leuconostoc/Radish Root Ferment Filtrate, Menthoxypropanediol, Phenoxyethanol, Selaginella Lepidophylla Extract, Sodium Hydroxide, Water.

Questions?

Question or comments? Call weekdays 9 AM to 6 PM PST at 1-877-786-2001 or email us at support@drnumb.com

— FDA label of Dr. Numb, Shinpharma Inc, effective April 30, 2026. 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.

Benzethonium chloride 170 mg/85 g · Lidocaine 3400 mg/85 g · aerosol, spray (topical) · 4 products

Drug Facts for this strength and form ↑

Brand or product nameCompany on the labelLabel
Blood Clotting HART Health DailyMed
Blood Clotting First Aid Unifirst First Aid Corporation DailyMed
Green Guard Super Stat Blood Clotting First Aid Unifirst First Aid Corporation DailyMed
Your Label Here Blood Clotting First Aid Dixon Investments, Inc. —
Benzethonium chloride 0.001 kg/kg · Lidocaine 0.04 kg/kg · gel (topical) · 1 product

Drug Facts for this strength and form ↑

Brand or product nameCompany on the labelLabel
Forticept Wounds and Burns Hydrogel Lidan, Inc. DailyMed
Benzethonium chloride 0.2 mg/100 mg · Lidocaine 4 mg/100 mg · aerosol, spray (topical) · 1 product

Drug Facts for this strength and form ↑

Brand or product nameCompany on the labelLabel
Super-Stop BloodClotter Cintas Corp DailyMed
Benzethonium chloride 0.25 mg/50 g · Lidocaine 4 mg/50 g · cream (topical) · 1 product

Drug Facts for this strength and form ↑

Brand or product nameCompany on the labelLabel
Dr. Numb Shinpharma 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.

  • Unifirst First Aid Corporation2 products
  • Dixon Investments, Inc.1 product
  • Lidan, Inc.1 product
  • HART Health1 product
  • Cintas Corp1 product
  • Shinpharma Inc1 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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