Moisture 002-01 and 002-02

MHS Moisturizing Hand Sanitizer by

Drug Labeling and Warnings

MHS Moisturizing Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Moisture 22 Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

MHS MOISTURIZING HAND SANITIZER- benzalkonium chloride liquid 
Moisture 22 Co., Ltd

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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Moisture 002-01 and 002-02

Active Ingredient(s)

Benzalkonium Chloride (0.05%)

Purpose

Antimicrobial

Use

For hand sanitizing to reduce bacteria on the skin.

Warnings

Do not use

If you are allergic to any of the ingredients.

Avoid getting into eyes (if contact occurs, wash well with clean water.

Do not mix with other chemicals.

Stop use andconsult a doctor if irritation or redness develops.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Place a small amount of the product onto the hands and rub hands together to spread evenly.

Other information

Properly stored in a cool, dry area, avoid direct sunlight. Store up to 5 years in a sealed container.

Inactive ingredients

Thymol, 2-Phenoxyethanol, Water, Glycerol, 1,2-Hexanediol, Aloe Barbadensis Leaf Juice, Chamomile Extract, Allantoin

Package Label - Principal Display Panel

500 mL NDC: 90014-002-02

MHS MOISTURIZING HAND SANITIZER 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 90014-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.05 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALLANTOIN (UNII: 344S277G0Z)
CHAMOMILE (UNII: FGL3685T2X)
GLYCERIN (UNII: PDC6A3C0OX)
HEXANEDIOL (UNII: ZIA319275I)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
THYMOL (UNII: 3J50XA376E)
PHENOXYETHANOL (UNII: HIE492ZZ3T)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 90014-002-02	500 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	07/31/2020
2	NDC: 90014-002-01	50 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	07/31/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	07/31/2020	12/01/2022

Labeler - Moisture 22 Co., Ltd (658294623)

Establishment
Name	Address	ID/FEI	Business Operations
Moisture 22 Co., Ltd		658294623	manufacture(90014-002)

Revised: 7/2023

Document Id: ffa08db7-7365-b8c0-e053-6294a90ad9de

34390-5

Set id: abb52a5a-71a8-5757-e053-2995a90af1e9

Version: 4

Effective Time: 20230703