Gentle Touch Foaming Hand Sanitizer

Gentle Touch Foaming Hand Sanitizer by

Drug Labeling and Warnings

Gentle Touch Foaming 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 FOAMING HAND SANITIZER- benzalkonium chloride 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.

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Gentle Touch Foaming Hand Sanitizer

Drug Facts

Active Ingredient

Benzalkonium Chloride 0.1%

Purpose

Antimicrobial

Uses

For hand sanitizing to decrease bacteria on the skin
Recommended for repeated use

Warnings

For external use only.   

When using this product

avoid contact with eyes. In case of eye contact, flush eyes with water.

Stop use and ask a doctor if

irritation or redness develops, or if condition persists for more than 72 hours.

KEEP OUT OF REACH OF CHILDREN.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Pump a small amount of foam into palm of hand

Rub thoroughly over all surfaces of both hands

Rub hands together briskly until dry.

Inactive Ingredients:

Water, cocamidopropyl PG-dimonium chloride phosphate, dihydroxyethyl cocamine oxide, acetamidoethoxyethanol, citric acid, fragrance

Package Labeling

GENTLE TOUCH FOAMING HAND SANITIZER 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78212-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)
DIHYDROXYETHYL COCAMINE OXIDE (UNII: 8AR51R3BL5)
ACETAMIDOETHOXYETHANOL (UNII: LVX2APC4XR)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78212-001-01	3785 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/27/2020	12/31/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	05/27/2020	12/31/2021

Labeler - Hill Chemical, Inc. (127089386)

Revised: 5/2021

Document Id: c200a13d-f912-32e3-e053-2995a90aee11

34390-5

Set id: a8369e41-63d4-63fd-e053-2995a90affad

Version: 2

Effective Time: 20210510