WET WIPE- wet wipes cloth

WET WIPE by

Drug Labeling and Warnings

WET WIPE by is a Otc medication manufactured, distributed, or labeled by Osike Cosmetics Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Benzalkonium Chloride 0.13% ……………………………………………...Antimicroblal

Purpose

Antimicroblal

Use

●Hand sanitizer to help reduce bacteria

●For use when soap and water are not available.

Warnings

For external use only.

Do not use

●in children less than 2 months old.

●on open skin wounds

WHEN USING

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

STOP USE

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.

Directions

●Apply to hands, allow to air dry without wiping.

●Children under 6 years of age should be supervised when using this product

Other information

●Store in a cool, dry place, between 15°C-30°C（59°F-86°F）

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

Inactive ingredients

Aloe Barbadensis Extract, Alpha-Tocopherol, Fragrance, Glycerin,

Phenoxyethanol, Propylene Glycol, Purified Water

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

WET WIPE 
wet wipes cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79866-010
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   in 100

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)
.ALPHA.-TOCOPHEROL, DL- (UNII: 7QWA1RIO01)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79866-010-01	40 in 1 DRUM; Type 0: Not a Combination Product	12/07/2020
2	NDC: 79866-010-02	75 in 1 DRUM; Type 0: Not a Combination Product	12/07/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	12/07/2020

Labeler - Osike Cosmetics Co., Ltd. (415803943)

Establishment
Name	Address	ID/FEI	Business Operations
Osike Cosmetics Co., Ltd.		415803943	manufacture(79866-010)