NON-ALCOHOL FOAMING HAND WASH- benzalkonium chloride 0.10% liquid

Non-Alcohol Foaming Hand Wash by

Drug Labeling and Warnings

Non-Alcohol Foaming Hand Wash by is a Otc medication manufactured, distributed, or labeled by Arkansas Correctional Industries, Allison Corbitt. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

12BENZALKONIUM CHLORIDE 0.10%

1 See: INNERMOST LABEL.jpg

2 See: OUTERMOST LABEL.jpg

DO NOT USE

Do not use in the eyes

STOP USE

Stop use and ask a doctor if irritation and/or redness occurs or if symptoms persist for more than 72 hours.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If ingested, seek medical attention or contact a Poison Control Center immediately.

PURPOSE

USE for waterless cleansing of hands to decrease soil on the skin

QUESTIONS

To obtain a copy of an SDS or for any questions or concerns, please call (877)635-7213 or visit our website: https://www.acicatalog.com/store/product_detail/753

WARNINGS

WARNINGS

For external use only

Do not use in the eyes

Stop use and ask a doctor if irritation and/or redness occurs or if symptoms persist for more than 72 hours.

Keep out of reach of children. If ingested, seek medical attention or contact a Poison Control Center immediately.

INACTIVE INGREDIENT

INACTIVE INGREDIENTS

Water, Laurtrimonium Chloride, Cetrimonium Chloride, Dihydroxyethyl Cocamine Oxide, Fragrance.

DOSAGE & ADMINISTRATION

DIRECTIONS

Place a palm full (approx. 5 grams) of product in one hand, spread on both hands, and rub into the skin until dry(approximately 1 to 2 minutes).
Place smaller amount (approx. 2.5 grams) into one hand, spread over both hands to wrist, and rub into the skin until dry(approximately 30 seconds).

INDICATIONS & USAGE

USE for waterless cleansing of hands to decrease soil on the skin

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

NON-ALCOHOL FOAMING HAND WASH 
benzalkonium chloride 0.10% liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78890-001
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
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)	0.01 g  in 100 mL
DIHYDROXYETHYL COCAMINE OXIDE (UNII: 8AR51R3BL5)	0.01 g  in 100 mL
WATER (UNII: 059QF0KO0R)	99.87 g  in 100 mL
LAURTRIMONIUM CHLORIDE (UNII: A81MSI0FIC)	0.01 g  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78890-001-01	3785 mL in 1 JUG; Type 0: Not a Combination Product	06/22/2020
2	NDC: 78890-001-02	208198 mL in 1 DRUM; Type 0: Not a Combination Product	06/22/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	06/22/2020

Labeler - Arkansas Correctional Industries (085528712)

Registrant - Allison Corbitt (085528712)

Establishment
Name	Address	ID/FEI	Business Operations
Arkansas Correctional Industries		085528712	manufacture(78890-001) , pack(78890-001) , label(78890-001)