V W- hand sanitizer wipe cloth

V W by

Drug Labeling and Warnings

V W by is a Otc medication manufactured, distributed, or labeled by Guangzhou Youxing Cosmetics CO.,LTD, Guangzhou Youxing Cosmetics CO.,LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Isopropyl alcohol 75% v/v

Purpose

Antimicrobial

Use

Hand sanitizer to help reduce bacteria on the skin

Warnings

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

WHEN USING

When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

STOP USE

Stop use and ask a doctor if irritation or rash appears and lasts

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

Wet hands thoroughly with product and allow to dry

Children under 6 years of age should be supervised when using wipe

Other information

Wet hands thoroughly with product and allow to dry

Children under 6 years of age should be supervised when using PURELL® products

Inactive ingredients

Water (Aqua), Isopropyl Alcohol, Glycerin, Aloe Barbadensis Leaf Juice, Isopropyl Myristate, Propylene Glycol, Retinyl Palmitate, Tocopheryl Acetate, Zea Mays (Corn) Oil

Package Label - Principal Display Panel

40 Cloth in one bag (​75239-007-01)

INGREDIENTS AND APPEARANCE

V W 
hand sanitizer wipe cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75239-007
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	75 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
CORN OIL (UNII: 8470G57WFM)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75239-007-01	100 mL in 1 BAG; Type 0: Not a Combination Product	07/17/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	07/17/2020

Labeler - Guangzhou Youxing Cosmetics CO.,LTD (544355953)

Establishment
Name	Address	ID/FEI	Business Operations
Guangzhou Youxing Cosmetics CO.,LTD.		544355953	manufacture(75239-007) , label(75239-007) , pack(75239-007)