FRESH HAND FOAMING HAND SANITIZER NON-ALCOHOL FOAM- benzalkonium chloride solution

FRESH HAND FOAMING HAND SANITIZER NON-ALCOHOL FOAM by

Drug Labeling and Warnings

FRESH HAND FOAMING HAND SANITIZER NON-ALCOHOL FOAM by is a Otc medication manufactured, distributed, or labeled by CWGC LA Inc., Guangzhou Gotdya Fine Chemical Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

BENZALKONIUM CHLORIDE 0.13%

Purpose

Antibacterial

PURPOSE

ANTIMICROBIAL

Use

• FOR HANDWASHING TO DECREASE BACTERIA ON THE SKIN. RECOMMENDED FOR REPEATED USE.

WARNINGS

For external use only.

WARNING: HARMFUL IF SWALLOWED.

CAUTION: KEEP OUT OF EYES. IN CASE OF ACCIDENTAL EYE CONTACT, FLUSH EYES THOROUGHLY WITH WATER. IF CONDITION WORSENS OR PERSISTS, CONTACT A PHYSICIAN. IF SWALLOWED, CONTACT A PHYSICIAN OR POISON CONTROL CENTER IMMEDIATELY.

When using this product

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

Keep out of reach of children.

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

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

DIRECTIONS

• APPLY FOAM SANITIZER TO HANDS AND RUB OVER SURFACES OF BOTH HANDS FOR 15 SECONDS. NO RINSING REQUIRED.

Inactive ingredients

WATER, COCO-GLUCOSIDE, LAURTRIMONIUM CHLORIDE, COCAMIDOPROPYLAMINE OXIDE, CITRIC ACID, FRAGRANCE.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

FRESH HAND FOAMING HAND SANITIZER NON-ALCOHOL FOAM 
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70415-204
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
COCO GLUCOSIDE (UNII: ICS790225B)
LAURTRIMONIUM CHLORIDE (UNII: A81MSI0FIC)
COCAMIDOPROPYLAMINE OXIDE (UNII: M4SL82J7HK)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70415-204-11	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/05/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	08/05/2020

Labeler - CWGC LA Inc. (034967904)