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Neutrogel Dailymed


Generic: soap

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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:
  • 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.
  • Glycerol (1.45% v/v).
  • Hydrogen peroxide (0.125% v/v).
  • 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

Otc - When Using Section


When using this product do not use
  • On children less than 2 months of age
  • On open skin wounds

Otc - Stop Use Section


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

Otc - Keep Out Of Reach Of Children Section


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

Recent Major Changes Section


Package Label - Principal Display Panel


4000 mL NDC: 77251-008-01

200000 mL NDC: 77251-008-02

20000 mL NDC : 77251-008-03

1000 mL NDC: 77251-008-04

500 mL NDC: 77251-008-05

250 mL NDC: 77251-008-06

DISCLAIMER:

"This tool does not provide medical advice, and is for informational and educational purposes only, and is not a substitute for professional medical advice, treatment or diagnosis. Call your doctor to receive medical advice. If you think you may have a medical emergency, please dial 911."

"Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service."

"This product uses publicly available data from the U.S. National Library of Medicine (NLM), National Institutes of Health, Department of Health and Human Services; NLM is not responsible for the product and does not endorse or recommend this or any other product."

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