RESPONSIBLE HAND SANITIZER

RESPONSIBLE HAND SANITIZER by

Drug Labeling and Warnings

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

Drug Details [pdf]

RESPONSIBLE HAND SANITIZER- ethyl alcohol gel 
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

Drug Facts

Active Ingredient

Ethyl Alcohol 70%

Purpose

Antiseptic

Use: Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings: For external use only. Flammable. Keep away from fire or flame.

Do not use on open skin wounds on children under the age of 2 months

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.

Directions Place enough product on hands to cover all surfaces. Rub hands together until dry.

Supervise children under 6 years of age when using this product to avoid swallowing.

Other Information Store between 59°-86°F (15°-30°C)

Avoid freezing and excessive heat above 104°F (40°C)

Inactive Ingredients purified water, glycerin, triethanolamine, carbomer, vitamin E

Advanced Moisturizing Formula with Vitamin E

Kills 99.99% of Germs

Made in PRC

Distributed by Clover Imaging Group

Hoffman Estates, IL 60169

Packaging

RESPONSIBLE HAND SANITIZER 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76720-003
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
TROLAMINE (UNII: 9O3K93S3TK)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
.ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76720-003-01	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/26/2020	07/29/2022
2	NDC: 76720-003-02	236 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/26/2020	07/29/2022
3	NDC: 76720-003-03	473 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/26/2020	07/29/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/26/2020	07/29/2022

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

Revised: 7/2022

Document Id: 55295f56-26a9-4a28-9bbf-0fb50b9c46f4

34390-5

Set id: 6173746f-dae3-40f9-8d45-2e29283c52ef

Version: 4

Effective Time: 20220713