BAYES Alcohol Free Foaming Hand Sanitizer Eucalyptus Lavender by LAB-CLEAN, INC

BAYES Alcohol Free Foaming Hand Sanitizer Eucalyptus Lavender by

Drug Labeling and Warnings

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

Drug Details [pdf]

BAYES ALCOHOL FREE FOAMING HAND SANITIZER EUCALYPTUS LAVENDER- benzalkonium chloride liquid 
LAB-CLEAN, INC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Active ingredient

Benzalkonium Chloride  0.1%

Purpose

Antimicrobial

Uses

For hand sanitizing to decrease bacteria on the 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

• Spray a small amount of product into the 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, Fragrance

Product label

BAYES ALCOHOL FREE FOAMING HAND SANITIZER EUCALYPTUS LAVENDER 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73126-036
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: 73126-036-01	59 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	06/11/2021
2	NDC: 73126-036-02	88 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	06/11/2021
3	NDC: 73126-036-03	236 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	06/11/2021
4	NDC: 73126-036-04	355 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	06/11/2021
5	NDC: 73126-036-05	946 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	06/11/2021
6	NDC: 73126-036-06	1890 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	06/11/2021
7	NDC: 73126-036-07	2000 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	06/11/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	06/11/2021	04/20/2024

Labeler - LAB-CLEAN, INC (199822219)

Establishment
Name	Address	ID/FEI	Business Operations
LAB-CLEAN, INC		199822219	manufacture(73126-036)

Revised: 4/2022

Document Id: dd9453da-9201-44f0-e053-2995a90a3e03

34390-5

Set id: 69ab85d7-359c-4062-aafa-d141be8d7247

Version: 2

Effective Time: 20220426