Label: HAND SANITIZER 72% ETHYL ALCOHOL liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 74311-175-08 - Packager: NZ Enterprises LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated April 15, 2020
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- Official Label (Printer Friendly)
- Purpose
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SPL UNCLASSIFIED SECTION
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.
- Do not use
- Other information
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WHEN USING
When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. - Active Ingredient(s)
- Warnings
- STOP USE
- Directions
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
HAND SANITIZER 72% ETHYL ALCOHOL
hand sanitizer 72% ethyl alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:74311-175 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 72 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) 0.26425 mL GLYCERIN (UNII: PDC6A3C0OX) 0.145 mL HYDROGEN PEROXIDE (UNII: BBX060AN9V) 0.0125 mL Product Characteristics Color Score Shape Size Flavor MANGO Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:74311-175-08 8 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/15/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 04/15/2020 Labeler - NZ Enterprises LLC (084052289) Registrant - NZ Enterprises LLC (084052289) Establishment Name Address ID/FEI Business Operations NZ Enterprises LLC 084052289 manufacture(74311-175)
