BAYES ALCOHOL FREE HYDRATING HAND SANITIZER- benzalkonium chloride spray

BAYES Alcohol free Hydrating Hand Sanitizer by

Drug Labeling and Warnings

BAYES Alcohol free Hydrating Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by LAB-CLEAN, INC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Benzalkonium Chloride  0.1%

Purpose

Antimicrobial

Uses

When using this product, avoid contact with eyes. In case of eye contact flush eyes with water. 

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

• Spray a small amount of product into palm of hand. Rub thoroughly over all surfaces of both hands.
• Rub hands together briskly until dry

Inactive ingredients

Water, Cetrimonium Chloride, Laurtrimonium Chloride, Dihydroxyethyl Cocamine Oxide, Glycereth-17 Cocoate, Citric Acid

Principal Display Panel

INGREDIENTS AND APPEARANCE

BAYES ALCOHOL FREE HYDRATING HAND SANITIZER 
benzalkonium chloride spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73126-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1 mg  in 1 mL

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73126-002-01	59 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	03/21/2020
2	NDC: 73126-002-02	88 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	03/21/2020
3	NDC: 73126-002-03	236 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	03/21/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	03/21/2020

Labeler - LAB-CLEAN, INC (199822219)

Establishment
Name	Address	ID/FEI	Business Operations
LAB-CLEAN, INC		199822219	manufacture(73126-002)