HAND SANITIZER- benzalkonium chloride solution
SNYDER MANUFACTURING CORP

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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SNYDER - SAFETOUCH HAND SANITIZER - BKC 0.1% (73038-103)

ACTIVE INGREDIENT

BENZALKONIUM CHLORIDE 0.1%

PURPOSE

ANTIMICROBIAL

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

USES

TO DECREASE BACTERIA ON THE SKIN THAT COULD CAUSE DISEASE 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.

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, DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE, GLYCERETH-2 COCOATE, BEHENTRIMONIUM CHLORIDE, DIHYDROXYETHYL COCAMINE OXIDE, FRAGRANCE

01b LBL (Front)_GSEP_Hand Sanitizer_BKC 01pct

01b LBL (DF Box)_GSEP_Hand Sanitizer_BKC 01pct

HAND SANITIZER
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:73038-103
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.1 g in 100 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE (UNII: 0Y0NQR2GH1)
GLYCERETH-2 COCOATE (UNII: JWM00VS7HC)
BEHENTRIMONIUM CHLORIDE (UNII: X7GNG3S47T)
DIHYDROXYETHYL COCAMINE OXIDE (UNII: 8AR51R3BL5)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:73038-103-11	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/12/2020	12/31/2021
2	NDC:73038-103-12	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/21/2020	12/31/2021
3	NDC:73038-103-13	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/21/2020	12/31/2021
4	NDC:73038-103-14	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/14/2020	12/31/2021

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	03/12/2020	12/31/2021

Labeler - SNYDER MANUFACTURING CORP (008277501)

Revised: 10/2021

Document Id: cf202472-00df-a5c6-e053-2a95a90adfdc

Set id: 10635562-efe6-4e7a-a866-b1b3328ad1d8

Version: 6

Effective Time: 20211024

SNYDER MANUFACTURING CORP