DISINFECTING WET WIPES patch

Disinfecting wet wipes by

Drug Labeling and Warnings

Disinfecting wet wipes by is a Otc medication manufactured, distributed, or labeled by Changzhou MeiMuSen New Material Technology Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Ethyl Alcohol(75%)
Benzalkonium Chloride(0.08%)

Purpose

Disinfection
Bacteriostat

Use

■Cleansing
■Disinfection
■Nursing

Warnings

Ask a doctor before use if you have
Patients with allergic skin Ask a doctor or pharmacist before use if you are
When using this product
Cleansing things
Disinfecting things
Travel period
Keep out of reach of the children.
Keep away from fire.

Do not use

/

WHEN USING

When using this product
Cleansing things
Disinfecting things
Travel period
Keep out of reach of the children.
Keep away from fire.

STOP USE

/

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of the children.

Directions

Tear Vnotch located on top of the plastic bag.
Place entire bag inside of center pull dispenser.
Close the lid of the dispenser.
Pullout the first wipes approximately 6 to 8 inches from the center of the roll.
Thread the wipe through the opening on the dispenser.
Wipedispensingtensionmaybe adjusted on the top of the dispenser.
Dispensermustbemountedwith wipes dispensing up.

Other information

store below 35℃(95℉)

Inactive ingredients

Cetylpyridinium Chloride, Didecyldimonium Chloride,
Glycerin, Aloe Barbadensis Leaf Extract,
Decylglucoside, Chamomilla Recutita Flower Extract, Aque

Package Label - Principal Display Panel

81838-001-01 50CLOTH in 1BAG

INGREDIENTS AND APPEARANCE

DISINFECTING WET WIPES 
disinfecting wet wipes patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81838-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	75 g  in 100
BENZALKONIUM (UNII: 7N6JUD5X6Y) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM	0.08 g  in 100

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P)
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
CHRYSANTHEMUM X MORIFOLIUM WHOLE (UNII: BEI52721UI)
DIDECYLDIMONIUM CHLORIDE (UNII: JXN40O9Y9B)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81838-001-01	50 in 1 BAG; Type 0: Not a Combination Product	03/30/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/30/2020

Labeler - Changzhou MeiMuSen New Material Technology Co., Ltd (715382258)

Establishment
Name	Address	ID/FEI	Business Operations
Changzhou MeiMuSen New Material Technology Co., Ltd		715382258	manufacture(81838-001)