Multi-purpose Antibacterial Wet Wipes by Supreme Premium Products,Inc.

Multi-purpose Antibacterial Wet Wipes by

Drug Labeling and Warnings

Multi-purpose Antibacterial Wet Wipes by is a Otc medication manufactured, distributed, or labeled by Supreme Premium Products,Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

MULTI-PURPOSE ANTIBACTERIAL WET WIPES- benzalkonium chloride cloth 
Supreme Premium Products,Inc.

----------

Drug Facts

Active Ingredient(s)

Benzalkonium Chloride 0.13%

Purpose

Antimicrobial Agent

Use

Decreases bacteria on skin.

Warnings

For external use only.

Do not use

Do not use if you are allergic to any of the ingredients.

Using this product do not get into eyes. lf contact occurs, rinse thoroughly with water.

Stop use and ask a doctor if irritation or rash develops and continues 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

Open using a label attached, pull out the wipe, and then seal the opening by sticking back the label to prevent the wipe from drying out.

Other information

The expiry date is stated on the packaging, Store at -20℃ to +30℃,away from sunlight.

Inactive ingredients

C12-14 Alkyl Dimethyl, Ethylbenzyl Ammonium Chloride, Alkyl Polyglucoside, Disodium EDTA, Propylene Glycol, Aqua.

Package Label - Principal Display Panel

MULTI-PURPOSE ANTIBACTERIAL WET WIPES 
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79531-003
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
EDETATE DISODIUM (UNII: 7FLD91C86K)
N-ALKYL ETHYLBENZYL DIMETHYL AMMONIUM CHLORIDE (C12-C14) (UNII: G258TFN61X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79531-003-01	77 g in 1 BAG; Type 0: Not a Combination Product	07/11/2020	12/31/2023
2	NDC: 79531-003-02	295 g in 1 BAG; Type 0: Not a Combination Product	07/11/2020	12/31/2023
3	NDC: 79531-003-03	435 g in 1 PAIL; Type 0: Not a Combination Product	07/11/2020	12/31/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	07/11/2020	12/31/2023

Labeler - Supreme Premium Products,Inc. (610328981)

Revised: 12/2025

Document Id: 472862de-ca58-ecd0-e063-6394a90afd26

34390-5

Set id: aa1e94f8-d808-1ad7-e053-2a95a90a3f94

Version: 2

Effective Time: 20251230