HAND SANITIZER- benzalkonium chloride solution

HAND SANITIZER by

Drug Labeling and Warnings

HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by SNYDER MANUFACTURING CORP. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

BENZALKONIUM CHLORIDE  0.1%

PURPOSE

ANTIMICROBIAL

KEEP OUT OF REACH OF CHILDREN

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HAND SANITIZER 
benzalkonium chloride solution

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

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

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

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

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

Labeler - SNYDER MANUFACTURING CORP (008277501)