Label: DISINFECTING WIPES- alcohol cloth
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Contains inactivated NDC Code(s)
NDC Code(s): 79681-004-01, 79681-004-02, 79681-004-03, 79681-004-04, view more79681-004-05, 79681-004-06 - Packager: Fuan HnH Bio Tech Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Export only
Drug Label Information
Updated July 26, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
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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.
- Active Ingredient(s)
- Purpose
- Use
- Warnings
- Do not use
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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. - STOP USE
- KEEP OUT OF REACH OF CHILDREN
- Directions
- Other information
- Inactive ingredients
- Package Label - Principal Display Panel
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INGREDIENTS AND APPEARANCE
DISINFECTING WIPES
alcohol clothProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79681-004 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength N-ALKYL ETHYLBENZYL DIMETHYL AMMONIUM CHLORIDE (C12-C14) (UNII: G258TFN61X) (N-ALKYL ETHYLBENZYL DIMETHYL AMMONIUM (C12-C14) - UNII:85440928RV) N-ALKYL ETHYLBENZYL DIMETHYL AMMONIUM CHLORIDE (C12-C14) 0.184 in 100 Inactive Ingredients Ingredient Name Strength N-ALKYL DIMETHYL BENZYL AMMONIUM CHLORIDE (C12-C18) (UNII: 9U1Q4T4ZYS) 0.184 WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79681-004-01 30 in 1 BAG; Type 0: Not a Combination Product 03/30/2020 2 NDC:79681-004-02 50 in 1 BAG; Type 0: Not a Combination Product 03/30/2020 3 NDC:79681-004-03 70 in 1 BAG; Type 0: Not a Combination Product 03/30/2020 4 NDC:79681-004-04 70 in 1 CANISTER; Type 0: Not a Combination Product 03/30/2020 5 NDC:79681-004-05 100 in 1 CANISTER; Type 0: Not a Combination Product 03/30/2020 6 NDC:79681-004-06 160 in 1 CANISTER; Type 0: Not a Combination Product 03/30/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date Export only 03/30/2020 Labeler - Fuan HnH Bio Tech Co., Ltd. (415711361) Establishment Name Address ID/FEI Business Operations Fuan HnH Bio Tech Co., Ltd. 415711361 manufacture(79681-004)
