NEWRAIN HAND SANITIZER- alcohol gel

NewRain Hand Sanitizer by

Drug Labeling and Warnings

NewRain Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Ganzhou Olivee Cosmetic Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Alcohol 75% ±5%

Purpose

 Antiseptic

Use(s)

Hand Sanitizer to help reduce bacteria that can potentially cause disease. For use when soap and water are not available.

Warnings

For external use only.

Flammable. Keep product away from fire or flame.

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

Stop use and ask a doctor if

irritation or redness develops and persists.

Other Information:

store between 15-30℃ (59-86℉)

avoid freezing and excssive heat above 40℃（104℉）.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Warning choking Hazard: Small Parts. Not intended for children under 3 years of age.

Directions

Wet hands thoroughly with product and rub hands together until dry.

Inactive ingredients

Alcohol Denat, Water (Aqua), Glycerin, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol

Packaging

INGREDIENTS AND APPEARANCE

NEWRAIN HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 56136-312
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)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
CARBOMER COPOLYMER TYPE A (UNII: 71DD5V995L)
.ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 56136-312-01	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/30/2020
2	NDC: 56136-312-02	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/30/2020
3	NDC: 56136-312-03	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/30/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	04/30/2020

Labeler - Ganzhou Olivee Cosmetic Co., Ltd. (543008195)

Registrant - Ganzhou Olivee Cosmetic Co., Ltd. (543008195)

Establishment
Name	Address	ID/FEI	Business Operations
Ganzhou Olivee Cosmetic Co., Ltd.		543008195	manufacture(56136-312)