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Neutrogel

Dosage form
GEL
Labeler
QUIMICA ROSMAR S.A DE C.V
Label updated
2021-01-12
Retrieved
2026-09-07
Active ingredients
BENZETHONIUM CHLORIDE
View original label and images on DailyMed ↗
Label information

This is a hand sanitizer manufactured according to the Temporary Policy for Preparation of Certain Alcohol-Based Hand Sanitizer Products During the Public Health Emergency (CoViD-19); Guidance for Industry.

The hand sanitizer is manufactured using only the following United States Pharmacopoeia (USP) grade ingredients in the preparation of the product (percentage in final product formulation) consistent with World Health Organization (WHO) recommendations:

  1. Alcohol (ethanol) (USP or Food Chemical Codex (FCC) grade) (80%, volume/volume (v/v)) in an aqueous solution denatured according to Alcohol and Tobacco Tax and Trade Bureau regulations in 27 CFR part 20.
  2. Glycerol (1.45% v/v).
  3. Hydrogen peroxide (0.125% v/v).
  4. Sterile distilled water or boiled cold water.

The firm does not add other active or inactive ingredients. Different or additional ingredients may impact the quality and potency of the product.

Active Ingredient(s)

Benzethonium chloride 0.10% w/w. Purpose: Antiseptic

Purpose

Antiseptic

Use
  • For washing sanitizing hands
  • Helps reduce bacteria on the skin that potentially can cause disease
Warnings

For external use only.

Do not use
  • in children less than 2 months of age
  • on open skin wounds
Label information

When using this product do not use

  • On children less than 2 months of age
  • On open skin wounds
Label information

Stop use and ask a doctor if irritation or redness persists for more than 72 hours.

Label information

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions
  • Wet as needed
  • Place enough product in your hand
  • Rub gently for at leats 30 seconds
  • Wash skin, rinse thoroughly and dry
Other information
  • Store at temperature below 110F (43C)
Inactive ingredients

water, sodium lauryl ether sulfate, cocamidopropyl betaine, cocamide DEA, glycerin, propylene glycol, sodium chloride, citric acid, DMDM hydantoin

Package Label - Principal Display Panel

[Image in the official label — see DailyMed source]

4000 mL NDC: 77251-008-01

200000 mL NDC: 77251-008-02

20000 mL NDC : 77251-008-03

[Image in the official label — see DailyMed source]

1000 mL NDC: 77251-008-04

[Image in the official label — see DailyMed source]

500 mL NDC: 77251-008-05

[Image in the official label — see DailyMed source]

250 mL NDC: 77251-008-06

[Image in the official label — see DailyMed source]

[Image in the official label — see DailyMed source]

DailyMed Set ID: b8421201-ea06-388d-e053-2995a90a2ecb · Version 1
NDC: 77251-008