CLEANSE-AF HAND SANITIZER- benzalkonium chloride liquid

Cleanse-AF Hand Sanitizer by

Drug Labeling and Warnings

Cleanse-AF Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by California Prison Industry Authority. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Benzalkonium chloride 0.1%

Purpose

Antimicrobial

Uses

Hand sanitzing to help reduce bacteria on skin.

Warnings

For external use only.

Ask doctor before use if you have

• Deep or puncture wounds
• Animal bites
• Serious burns

When using this product

• Avoid contact with eyes
• In case of contact, flush eyes with water
• Do not ingest

Stop use and ask doctor

If redness or irritation develops and persists. These may be signs of a serious condition.

Keep out of reach of children

Children should be supervised when using this product. If swallowed call a Poison Control Center or get medical help right away.

Directions

• Pump a small amount of foam into palm of hand. Rub thoroughly over all surfaces of both hands. Rub hands briskly until dry.
• Supervise children under 6 years of age when using this product to avoid swallowing.

Inactive ingredients

Cetrimonium chloride, citric acid, dihydroxyethyl cocamine oxide, glycereth-17 cocoate, lautrimonium chloride, water.

Label

INGREDIENTS AND APPEARANCE

CLEANSE-AF HAND SANITIZER 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74966-004
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 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERETH-17 COCOATE (UNII: 3057VPT0KC)
LAURTRIMONIUM CHLORIDE (UNII: A81MSI0FIC)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
WATER (UNII: 059QF0KO0R)
DIHYDROXYETHYL COCAMINE OXIDE (UNII: 8AR51R3BL5)
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74966-004-16	473.176 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	06/04/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	06/04/2021

Labeler - California Prison Industry Authority (843406104)

Establishment
Name	Address	ID/FEI	Business Operations
California Prison Industry Authority		843406104	manufacture(74966-004) , label(74966-004) , pack(74966-004)