Gentle Touch Antibacterial Hand Sanitizer

Gentle Touch Antibacterial Hand Sanitizer by

Drug Labeling and Warnings

Gentle Touch Antibacterial Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Hill Chemical, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

GENTLE TOUCH ANTIBACTERIAL HAND SANITIZER- alcohol liquid 
Hill Chemical, 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.

----------

Gentle Touch Antibacterial Hand Sanitizer

Drug Facts

Active Ingredient

Ethyl Alcohol 72.38%

Purpose

Antimicrobial

Uses

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

Warnings

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

When using this product

do not use it 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

Put enough product in your palm to cover hands and rub hands together briskly until dry.

Children under 6 years of age should be supervised when using this product.

Inactive Ingredients:

Glycerin, Hydrogen Peroxide, Purified Water USP.

Package Labeling

GENTLE TOUCH ANTIBACTERIAL HAND SANITIZER 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78212-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.7238   in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
HYDROGEN PEROXIDE (UNII: BBX060AN9V)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78212-002-01	3785 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/12/2020	12/31/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	06/12/2020	12/31/2021

Labeler - Hill Chemical, Inc. (127089386)

Revised: 5/2021

Document Id: c200a13d-f90f-32e3-e053-2995a90aee11

34390-5

Set id: a836a826-e5cd-1b1f-e053-2995a90a1379

Version: 2

Effective Time: 20210510