HAND SANITIZER- alcohol gel

HAND SANITIZER by

Drug Labeling and Warnings

HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by NingBo Huize Commodity Co.,Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethyl Alcohol 62%

Purpose

Antiseptic

Use

Decreases bacteria on hands

Warning

for external use only

Do not use on broken skin & around eyes

When using this product
■Keep away from fire or flame
■Using other topical acne drugs at the same time or right after use of this product may increase dryness or irritation of the skin . Only one drug should be used unless directed by a doctor.

Keep out of reach of children

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

Directions

Squeeze onto hands and rub hands and rub hands together briskly until dry

INACTIVE INGREDIENT

Deionized Water, glycerin , Propylene Glycol, aloe vera gel,fragrance,DMDMH

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71011-003
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)
DMDM HYDANTOIN (UNII: BYR0546TOW)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
PROPYLENE GLYCOL DIACETATE (UNII: 5Z492UNF9O)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71011-003-01	5 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/20/2016
2	NDC: 71011-003-02	8 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/20/2016
3	NDC: 71011-003-03	10 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/20/2016
4	NDC: 71011-003-04	15 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/20/2016
5	NDC: 71011-003-05	20 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/19/2016
6	NDC: 71011-003-06	30 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/19/2016
7	NDC: 71011-003-07	50 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/20/2016
8	NDC: 71011-003-08	60 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/20/2016
9	NDC: 71011-003-09	80 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/20/2016
10	NDC: 71011-003-10	100 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/20/2016
11	NDC: 71011-003-11	150 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/20/2016
12	NDC: 71011-003-12	200 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/20/2016
13	NDC: 71011-003-13	250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/20/2016
14	NDC: 71011-003-14	300 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/20/2016
15	NDC: 71011-003-15	400 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/20/2016
16	NDC: 71011-003-16	500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/20/2016
17	NDC: 71011-003-17	600 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/20/2016
18	NDC: 71011-003-18	700 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/20/2016
19	NDC: 71011-003-19	800 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/20/2016
20	NDC: 71011-003-20	900 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/20/2016
21	NDC: 71011-003-21	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/20/2016
22	NDC: 71011-003-22	2000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/20/2016
23	NDC: 71011-003-23	5 mL in 1 POUCH; Type 0: Not a Combination Product	10/20/2016
24	NDC: 71011-003-24	8 mL in 1 POUCH; Type 0: Not a Combination Product	10/20/2016
25	NDC: 71011-003-25	25 mL in 1 POUCH; Type 0: Not a Combination Product	10/20/2016
26	NDC: 71011-003-26	15 mL in 1 POUCH; Type 0: Not a Combination Product	10/20/2016
27	NDC: 71011-003-27	20 mL in 1 POUCH; Type 0: Not a Combination Product	10/20/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/09/2016

Labeler - NingBo Huize Commodity Co.,Ltd. (544434795)

Establishment
Name	Address	ID/FEI	Business Operations
NingBo Huize Commodity Co.,Ltd.		544434795	manufacture(71011-003)