Molchem hand purifier by MOL BELTING SYSTEMS, INC / Mol Belting Systems Inc

Molchem hand purifier by

Drug Labeling and Warnings

Molchem hand purifier by is a Otc medication manufactured, distributed, or labeled by MOL BELTING SYSTEMS, INC, Mol Belting Systems Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

MOLCHEM HAND PURIFIER- benzalkonium chloride spray 
MOL BELTING SYSTEMS, INC

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Warnings

For external use only.

When using this productkeep out of eyes, ears and mouth. In case of contact with eyes, rinse thoroughly
with water.

Stop use and ask a doctorif irritation or rash occurs. This may be a sign of a serious condition.

Keep out of reach of children.

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

Other information

Store in dry place between 35° and 103°F

Directions

Place enough product on hands to cover all surfaces. Rub hands together.

Supervise children under 6 years of age when using this product to avoid swallowing.

Uses

To decrease bacteria on the skin.

Recommended for repeated use.

For use when soap and water are not available

Inactive ingredients

Deionized Water, Propylene glycol, Triethylene glycol, Phospholipids Complex, Organo Silane Quaternaries

Active ingredient

Benzalkonium Chloride 0.13%

Purpose

Antiseptic

Product label

MOLCHEM HAND PURIFIER 
benzalkonium chloride spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80606-001
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
DIMETHYLOCTADECYL(3-(TRIMETHOXYSILYL)PROPYL)AMMONIUM CHLORIDE (UNII: IQ36O85WQ4)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
TRIETHYLENE GLYCOL (UNII: 3P5SU53360)
PEG-75 LANOLIN (UNII: 09179OX7TB)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80606-001-01	59.14 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	07/15/2021	10/29/2024
2	NDC: 80606-001-02	236.58 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	07/15/2021	10/29/2024
3	NDC: 80606-001-03	3785.41 mL in 1 DRUM; Type 0: Not a Combination Product	07/15/2021	10/29/2024
4	NDC: 80606-001-04	18927.1 mL in 1 DRUM; Type 0: Not a Combination Product	07/15/2021	10/29/2024
5	NDC: 80606-001-05	208198 mL in 1 DRUM; Type 0: Not a Combination Product	07/15/2021	10/29/2024
6	NDC: 80606-001-06	1040987.75 mL in 1 JUG; Type 0: Not a Combination Product	07/15/2021	10/29/2024
7	NDC: 80606-001-07	500 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	07/15/2021	10/29/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	07/15/2021	10/29/2024

Labeler - MOL BELTING SYSTEMS, INC (147753685)

Establishment
Name	Address	ID/FEI	Business Operations
Mol Belting Systems Inc		147753685	pack(80606-001)

Revised: 12/2024

Document Id: 2a49ea0f-d6fd-b0d8-e063-6394a90aed64

34390-5

Set id: 303b5ce9-9715-4291-a899-649d1d70fc95

Version: 5

Effective Time: 20241227