STERILIZED WET WIPES dressing

Sterilized wet wipes by

Drug Labeling and Warnings

Sterilized wet wipes by is a Otc medication manufactured, distributed, or labeled by JINGXIN GROUP (M) SDN BHD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

BENZALKONIUM CHLORIDE

PURPOSE

Antiseptic, Hand Sanitizer

INDICATIONS & USAGE

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

WARNINGS

For external use only. Flammable. Keep away from heat or flame.

DO NOT USE

in children less than 2 months of age.

on open shin wounds.

WHEN USING

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thouroughly with water.

STOP USE

Stip use and ack a doctor if irritation or rash occurs. These may be signs of a serious condition.

KEEP OUT OF REACH OF CHILDREN

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

DOSAGE & ADMINISTRATION

Place enough product on hands to cover all surfaces.

STORAGE AND HANDLING

Store between 15-30C (59-86F).

Avoid freezing and excessive heat above 40C (104F).

INACTIVE INGREDIENT

CELLULOSE, WATER, CETYLPYRIDINIUM CHLORIDE, BENZETHONIUM CHLORIDE, PROPYLENE GLYCOL

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

STERILIZED WET WIPES 
sterilized wet wipes dressing

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85868-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP)	BENZETHONIUM CHLORIDE	0.0018 g  in 1 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)	0.9967 g  in 1 g
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)	0.0015 g  in 1 g

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85868-001-02	80 in 1 PATCH	07/07/2025
1	NDC: 85868-001-01	3.3 g in 1 PATCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M007	07/07/2025

Labeler - JINGXIN GROUP (M) SDN BHD (965305544)

Registrant - JINGXIN GROUP (M) SDN BHD (965305544)

Establishment
Name	Address	ID/FEI	Business Operations
JINGXIN GROUP (M) SDN BHD		965305544	manufacture(85868-001)