SANIXUSA HAND SANITIZER- ethyl alcohol 75% gel

Sanixusa Hand Sanitizer by

Drug Labeling and Warnings

Sanixusa Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by GUANGZHOU RAINHOME PHARM&TECH CO., LTD, Chilla Beverages USA. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethyl Alcohol 75%

­­­­­­­­­­­­­­­­­­­­­ Purpose

Antiseptic

Uses

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

Warnings

For External Use Only. FLAMMABLE. Keep away from heat or flame.

Do not use

In children less than 2 months of age. On open skin wounds.

When using this product

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

­­­­­­­­­­­­­­­­­­­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.

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

­­­­­­­­­­­­­­­­­­­­­Directions

Place enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 6 years of age when using this product to avoid swallowing

Other Information

Store between 15-30C (59-85F).

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

Inactive Ingredients

Water, C10 30 alkyl acrylate crosspolymer, aminomethyl propanol, glycerin, aloe barbadensis (leaf) extract

Sanixusa Hand Sanitizer

INGREDIENTS AND APPEARANCE

SANIXUSA HAND SANITIZER 
ethyl alcohol 75% gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78126-110
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)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78126-110-03	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/01/2020
2	NDC: 78126-110-02	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/01/2020
3	NDC: 78126-110-06	200 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/01/2020
4	NDC: 78126-110-16	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/01/2020
5	NDC: 78126-110-33	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/01/2020

Labeler - GUANGZHOU RAINHOME PHARM&TECH CO., LTD (547018779)

Registrant - Chilla Beverages USA (078572585)