RESPONSIBLE HAND SANITIZER WIPES

Responsible by

Drug Labeling and Warnings

Responsible by is a Otc medication manufactured, distributed, or labeled by General Printing & Design, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

RESPONSIBLE- alcohol swab 
General Printing & Design, Inc.

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.

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RESPONSIBLE HAND SANITIZER WIPES

Drug Facts

Active ingredient

Alcohol 75% by volume

Purpose

Antiseptic

Uses  For hand washing to decrease bacteria on the skin. Apply topically to the skin to help prevent cross contamination. Recommended for repeated use. Dries in seconds when used as directed.

Warnings Flammable, keep away from fire or flame. For external use only. When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water. Stop use and ask a doctor if irritation or rash appears and lasts.

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

Directions  To Open Package: Unscrew lid to remove. Open foil bag. Locate wipe in the center and insert corner of the wipe through opening in lid. DO NOT PUSH FINGER THROUGH OPENING. Replace lip. Pull sheet up slightly to side. Always snap lid cap securely shut between uses to prevent moisture loss.  Use wipe to thoroughly wipe hands, fingers, and wrists. Be sure to use the entire wipe. Allow to dry.  For dirty hands, use first wipe to clean hands, then discard wipe; sanitize with second wipe.  Discard after single use – Do not flush. 

Inactive ingredients Water, Chlorhexidine Diacetate, Benzalkonium Chloride, Nano Silver Ions, Vitamin E

Advanced Moisturizing Formula with Vitamin E

Kills 99.9% of Germs

Distributed by Clover Imaging Group

Hoffman Estates, IL 60169

MADE IN CHINA

Packaging

RESPONSIBLE 
alcohol swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76720-011
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	75 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CHLORHEXIDINE ACETATE (UNII: 5908ZUF22Y)
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
SILVER CATION (UNII: 57N7B0K90A)
.ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76720-011-01	20 in 1 BAG	06/04/2020	07/29/2022
1		5.29 mL in 1 PACKAGE; Type 0: Not a Combination Product
2	NDC: 76720-011-02	100 in 1 CANISTER	06/04/2020	07/29/2022
2		5.29 mL in 1 PACKAGE; Type 0: Not a Combination Product
3	NDC: 76720-011-03	80 in 1 BAG	06/04/2020	07/29/2022
3		5.29 mL in 1 PACKAGE; Type 0: Not a Combination Product
4	NDC: 76720-011-04	700 in 1 CANISTER	06/04/2020	07/29/2022
4		5.29 mL in 1 PACKAGE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/04/2020	07/29/2022

Labeler - General Printing & Design, Inc. (066630757)

Revised: 7/2022

Document Id: 39d77c4d-1055-48f9-b088-1e599bf432cc

34390-5

Set id: fa687510-ad08-4ae8-9f47-db6178cb8d44

Version: 4

Effective Time: 20220713