WET WIPES- disinfectant wipes cloth

Wet Wipes by

Drug Labeling and Warnings

Wet Wipes by is a Otc medication manufactured, distributed, or labeled by Anhui Hanbon Daily Chemical Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Glycerol

PURPOSE

Disinfection
Sterilization
No Rinseing

WARNINGS

Open the lid, tear off the label, then take it out directly for use. After use, please close the
lidfirmly in time to avoid the wipes drying out.

DOSAGE & ADMINISTRATION

Please keep it out of reach of children to avoid accidental eating.
Keep it in a cool place, not under direct sunlight.
Please stop using it and consult a doctor if you feel sensitive or not well.

KEEP OUT OF REACH OF CHILDREN

keep out of reach of children

INACTIVE INGREDIENT

Deionized water,propylene glycol,Aloe Barbadensis Leaf Extract,Benzalkonium chloride,Chamomilla recutita flower extract,Didecyldimonium Chloride,C12-14 alkyl dimethyl ethylbenzyl ammonium chloride,Tea tree oil,Citric Acid

INDICATIONS & USAGE

cleaning human skin, hands and object surface, avoiding using it on eyes, wounds and other sensitive areas.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

WET WIPES 
disinfectant wipes cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 40562-007
Route of Administration	EXTRACORPOREAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX)	GLYCERIN	0.21   in 70

Inactive Ingredients
Ingredient Name	Strength
TEA TREE OIL (UNII: VIF565UC2G)
CHAMOMILE (UNII: FGL3685T2X)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)
N-ALKYL ETHYLBENZYL DIMETHYL AMMONIUM CHLORIDE (C12-C14) (UNII: G258TFN61X)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
DIDECYLDIMONIUM CHLORIDE (UNII: JXN40O9Y9B)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)

Product Characteristics
Color		Score
Shape		Size
Flavor		Imprint Code	kidclean
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 40562-007-01	40 in 1 BLISTER PACK; Type 0: Not a Combination Product	04/21/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		04/21/2020

Labeler - Anhui Hanbon Daily Chemical Co., Ltd. (405624856)

Establishment
Name	Address	ID/FEI	Business Operations
Anhui Hanbon Daily Chemical Co., Ltd.		405624856	manufacture(40562-007)