DR. BANCROFT'S GEL HAND SANITIZER

Dr. Bancrofts Gel Hand Sanitizer by

Drug Labeling and Warnings

Dr. Bancrofts Gel Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Sazerac Company, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DR. BANCROFTS GEL HAND SANITIZER- alcohol gel 
Sazerac Company, 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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DR. BANCROFT'S GEL HAND SANITIZER

Drug Facts

Active Ingredient([s]

Denatured Alcohol 70% v/v

Purpose

Antiseptic

Use[s]  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 heat or flame

Do not use  on children less than 2 months of age on open skin wounds

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 15-30C (59-86F)
• Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

aminomethylpropanol, carbomer, purified water

Principal Display Panel

FREE OF FRAGRANCES AND DYES

Dr. Bancroft's

HAND
SANITIZER

PROUDLY MADE IN THE U.S.A.

ALCOHOL ANTISEPTIC 70%
TOPICAL SOLUTION
NON-STERILE SOLUTION

3.4 FL OZ (100 mL)

MANUFACTURED BY SAZERAC COMPANY 10101 LINN STATION ROAD
LOUISVILLE, KY 40223 QUESTIONS? 866-729-3722

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DR. BANCROFTS GEL HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75089-301
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
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75089-301-05	100 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/21/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	07/21/2020	12/01/2022

Labeler - Sazerac Company, Inc. (078761784)

Registrant - Sazerac Company, Inc. (078761784)

Revised: 12/2022

Document Id: 076a1cb7-d7b2-45d1-949b-500ca9dc625d

34390-5

Set id: 3016c084-1bd3-40b1-8050-f38d80ec6211

Version: 2

Effective Time: 20221228