ANTIBACTERIAL HAND SANITIZER- ethyl alcohol spray

Antibacterial Hand Sanitizer by

Drug Labeling and Warnings

Antibacterial Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Zhejiang Ayan Biotech Co.,Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredients

Ethyl Alcohol 62%

Purpose

Antiseptic

Uses:

Hand sanitizer to help decrease bacteria on the skin. When water, soap & towel are not available. Recommended for repeated use.

Warnings:

For external use only.

Flammable. Keep away from fire or flame.

Do not apply around eyes, Do not use in ears & mouth.

When using this product,

avoid contact with eyes. In case of contact flush eyes with water.

Stop use and ask a doctor

if redness or irritation develop and persist for more than 72 hours.

Keep out of reach of children.

Children must be supervised in use of this product.

Directions:

Squits as needed into your palms and thoroughly spread on both hands. Rub into skin until dry

Other Information:

Store at 20° C (68° to 77°F). May discolor fabrics

Inactive Ingredients

water, triethanolamine, glycerin, propylene glycol, tocopheryl acetate, carbomer, fragrance.

Package Labeling:

INGREDIENTS AND APPEARANCE

ANTIBACTERIAL HAND SANITIZER 
ethyl alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70412-119
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	620 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
TROLAMINE (UNII: 9O3K93S3TK)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70412-119-03	1 in 1 BOX	01/18/2016
1		3 mL in 1 BOTTLE; Type 0: Not a Combination Product
2	NDC: 70412-119-05	1 in 1 BOX	01/18/2016
2		5 mL in 1 BOTTLE; Type 0: Not a Combination Product
3	NDC: 70412-119-08	1 in 1 BOX	01/18/2016
3		8 mL in 1 BOTTLE; Type 0: Not a Combination Product
4	NDC: 70412-119-10	1 in 1 BOX	01/18/2016
4		10 mL in 1 BOTTLE; Type 0: Not a Combination Product
5	NDC: 70412-119-12	1 in 1 BOX	01/18/2016
5		12 mL in 1 BOTTLE; Type 0: Not a Combination Product
6	NDC: 70412-119-16	1 in 1 BOX	01/18/2016
6		16 mL in 1 BOTTLE; Type 0: Not a Combination Product
7	NDC: 70412-119-20	1 in 1 BOX	01/18/2016
7		20 mL in 1 BOTTLE; Type 0: Not a Combination Product
8	NDC: 70412-119-25	1 in 1 BOX	01/18/2016
8		25 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	01/18/2016

Labeler - Zhejiang Ayan Biotech Co.,Ltd. (544377996)