FOAMING HAND SANITIZER- hand sanitizer liquid

Foaming Hand Sanitizer by

Drug Labeling and Warnings

Foaming Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by American Chemical Systems II, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Drug Facts

Active ingredient
Benzalkonium chloride .13%.......Antibacterial

PURPOSE

Purpose
Antibacterial

INDICATIONS & USAGE

Uses

hand sanitizer to decrease bacteria on the skin

WARNINGS

Warnings

For external use only

When using this product do not get
into eyes. In case of contact, rinse eyes thoroughly with water

Stop use and ask a doctor if
irritation or redness develop and condition
persists.

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.

DOSAGE & ADMINISTRATION

Directions
wet hands thoroughly with product and
   allow to dry without wiping
supervise children when using this product

INACTIVE INGREDIENT

Inactive ingredients Purified Water, Aloe Vera, Propylene Glycol, Triethylene Glycol, Polysorbate-20, Fragrance

ACS™ FOAMING HAND SANITIZER Labeling

ACS™

FOAMING
HAND

SANITIZER

Distributed by:
AMERICAN CHEMICAL SYSTEMS II, LLC
2520 South Sheridan St.,
Wichita, Kansas 67217
(800) 889-3489

Lot No:
Expiry

Labeling [2 x 1 gal. (7.6 L)]

Labeling [3-33.8 fl oz (1 L) Bottles (101.4 fl oz (3 qt 5.4 fl oz) (3 L))]

rege

INGREDIENTS AND APPEARANCE

FOAMING HAND SANITIZER 
hand sanitizer liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75044-280
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.3 g  in 1000 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALOE VERA FLOWER (UNII: 575DY8C1ER)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
TRIETHYLENE GLYCOL (UNII: 3P5SU53360)
POLYSORBATE 20 (UNII: 7T1F30V5YH)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75044-280-31	3 in 1 CASE	09/01/2024
1		1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
2	NDC: 75044-280-16	2 in 1 CASE	09/01/2024
2		3800 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	09/01/2024

Labeler - American Chemical Systems II, LLC (016631058)