HYGIENE CLEAN LEATHER OAK HAND SANITIZER- benzalkonium chloride liquid

Hygiene Clean Leather Oak Hand Sanitizer by

Drug Labeling and Warnings

Hygiene Clean Leather Oak Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by USA Broom LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

Antimicrobial

Uses

• For hand sanitizing to decrease the bacteria on skin.
• 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.

KEEP OUT OF REACH OF CHILDREN.

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

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; Propylene Glycol; Lauramine Oxide; Undeceth-7; Disodium EDTA; Aloe Barbadensis Gel; Glycereth-2-Cocoate; DMDM Hydantoin; Fragrance, Citric Acid

Package Labeling:50ml

Package Labeling:50ml 24 bottles

INGREDIENTS AND APPEARANCE

HYGIENE CLEAN LEATHER OAK HAND SANITIZER 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80499-010
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 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
UNDECETH-7 (UNII: R6B5PCO2JN)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERETH-2 COCOATE (UNII: JWM00VS7HC)
DMDM HYDANTOIN (UNII: BYR0546TOW)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80499-010-01	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/30/2020
2	NDC: 80499-010-02	24 in 1 BOX	10/30/2020
2		50 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	10/30/2020

Labeler - USA Broom LLC (117638854)