ALLPEAU PURE HAND SANITIZER- alcohol hand sanitizer gel

allpeaU Pure Hand Sanitizer by

Drug Labeling and Warnings

allpeaU Pure Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by WID Cosmetics (Shanghai) Co., Ltd., A03 Lab of BTS. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Alcohol 75% v/v. Purpose: Hand Sanitizer

Purpose

Hand Sanitizer

Use

Hand sanitizer to decrease on hands.

Warnings

• For external use only.
• Flammable. Keep away from heat and flame.

Do not use

Do not use in the eyes. In case of contact, rinse eyes thoroughly with water.

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 and redness develops and lasts.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help immediately.

Directions

• Take proper amount of product into the palm and rub hands together until dry.
• Supervise children under 6 years in the use of the product. Not recommended for infants.

Other information

Store below 110℉ (43℃).

May discolor certain fabrics or surfaces.

Inactive ingredients

water, acrylates/vinyl isodecanoate crosspolymer, propylene glycol, triethanolamine, aloe barbadensis extract, cucumis sativus extract, houttuynia cordata extract, parfum, CI 42090, CI 19140

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

ALLPEAU PURE HAND SANITIZER 
alcohol hand sanitizer gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75567-1011
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	42 mL  in 60 mL

Inactive Ingredients
Ingredient Name	Strength
HOUTTUYNIA CORDATA FLOWERING TOP (UNII: RH041UUZ22)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
CUCUMBER (UNII: YY7C30VXJT)
TROLAMINE (UNII: 9O3K93S3TK)
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW) (UNII: JZ1374NL9E)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75567-1011-1	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/27/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/27/2020

Labeler - WID Cosmetics (Shanghai) Co., Ltd. (554443373)

Registrant - A03 Lab of BTS (548009541)

Establishment
Name	Address	ID/FEI	Business Operations
WID Cosmetics (Shanghai) Co., Ltd.		554443373	manufacture(75567-1011) , label(75567-1011)