COLORROSE HAND SANITIZER- alcohol gel

Colorrose Hand Sanitizer by

Drug Labeling and Warnings

Colorrose Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Zhejiang Cheerflor Cosmetics Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

[Active ingredient]

Alcohol 75% v/v

[Purpose]

Sterilization

[Inactive ingredients]

Aqua, Acrylates/C10-30 alkyl Acrylate Crosspolymer, Triethanolamine, Glycerin, Propylene Glycol, Aloe Vera Extract.

[Use]

Hand disinfection. Helps reduce bacteria on the skin and kills most common germs that may cause illness.

[Directions]

Place enough product in your palm to thoroughly cover your hands. Rub hands together briskly until dry. Children under 6 years of age should be supervised when using this product.

[Warnings]

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

3.When using this product

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

Stop use and ask a doctor

if irritation on rash appears and lasts.

4.Keep out of reach of children.

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

SPL UNCLASSIFIED SECTION

5.Store below 110 degrees F [43 degrees C].

Package and Labeling 30ml

Package and Labeling 50ml

Package and Labeling 60ml

Package and Labeling 100ml

Package and Labeling 240ml

Package and Labeling 300ml

Package and Labeling 500ml

Package and Labeling 1000ml

INGREDIENTS AND APPEARANCE

COLORROSE HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78163-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.75 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
TROLAMINE (UNII: 9O3K93S3TK)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78163-001-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/20/2020
2	NDC: 78163-001-02	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/20/2020
3	NDC: 78163-001-03	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/20/2020
4	NDC: 78163-001-04	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/20/2020
5	NDC: 78163-001-05	240 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/20/2020
6	NDC: 78163-001-06	300 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/20/2020
7	NDC: 78163-001-07	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/20/2020
8	NDC: 78163-001-08	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/20/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	05/20/2020

Labeler - Zhejiang Cheerflor Cosmetics Co., Ltd. (529325329)