HAND SANITIZER- alcohol liquid

HAND SANITIZER by

Drug Labeling and Warnings

HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by Deqing Jiarou Daily Chemical Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Alcohol 62 %

Purpose

Antiseptic

Uses

Decreases Bacteria on Hands

Warning

Flammable. Keep away from fire or flame

For external use only.

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

Discontinue use if irritation or redness develops. If condition persists for more than 72 hours, consult a doctor.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

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.

Inactive ingredients

PURIFIED WATER, GLYCERIN, TRIETHANOLAMINE, CARBOMER, FRAGRANCE, VITAMIN E, ALOE VERA.

SPL UNCLASSIFIED SECTION

Made in China

Packaging

INGREDIENTS AND APPEARANCE

HAND SANITIZER 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70675-958
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
TROLAMINE (UNII: 9O3K93S3TK)
CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
.ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70675-958-01	8 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/12/2016
2	NDC: 70675-958-02	10 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/12/2016
3	NDC: 70675-958-03	15 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/12/2016
4	NDC: 70675-958-04	20 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/12/2016
5	NDC: 70675-958-66	29 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/16/2017
6	NDC: 70675-958-05	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/12/2016
7	NDC: 70675-958-06	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/12/2016
8	NDC: 70675-958-07	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/12/2016
9	NDC: 70675-958-21	75 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/16/2017
10	NDC: 70675-958-08	80 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/12/2016
11	NDC: 70675-958-23	90 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/16/2017
12	NDC: 70675-958-09	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/12/2016
13	NDC: 70675-958-10	120 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/12/2016
14	NDC: 70675-958-24	350 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/16/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/12/2016

Labeler - Deqing Jiarou Daily Chemical Co., Ltd (544398724)

Establishment
Name	Address	ID/FEI	Business Operations
Deqing Jiarou Daily Chemical Co., Ltd		544398724	manufacture(70675-958)