ANTISEPTIC CLEANING WIPE patch

Antiseptic Cleaning wipe by

Drug Labeling and Warnings

Antiseptic Cleaning wipe by is a Otc medication manufactured, distributed, or labeled by SHENZHEN BENLIJU BIO-TECH CO.,LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

benzalkonium chloride ,chlorhexidine

PURPOSE

disinfect

INDICATIONS & USAGE

For Daily cleaning and disinfecting care wipe for human skin or object surface.

WARNINGS

*For extemal use only.
*Flammable. keep away from fire or flame.

DO NOT USE

Do not use " with electrocautery procedures " in the eyes. lf contact occurs, flush eyes with water.

WHEN USING

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

STOP USE

*Stop use if irritation and redness develop. If condition persists consult your health care practioner.

*Stop use and ask 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

For Daily cleaning and disinfecting care wipe for human skin or object surface.One piece at a time.

STORAGE AND HANDLING

Store at room temperature.

INACTIVE INGREDIENT

water,phenoxyethanol

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ANTISEPTIC CLEANING WIPE 
antiseptic cleaning wipe patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84449-004
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	4 mg  in 1 g
CHLORHEXIDINE (UNII: R4KO0DY52L) (CHLORHEXIDINE - UNII:R4KO0DY52L)	CHLORHEXIDINE	10 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
PHENOXYETHANOL (UNII: HIE492ZZ3T)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84449-004-01	1 g in 1 PATCH; Type 0: Not a Combination Product	08/22/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	08/22/2024

Labeler - SHENZHEN BENLIJU BIO-TECH CO.,LTD (551073413)

Registrant - SHENZHEN BENLIJU BIO-TECH CO.,LTD (551073413)

Establishment
Name	Address	ID/FEI	Business Operations
SHENZHEN BENLIJU BIO-TECH CO.,LTD		551073413	manufacture(84449-004)