HAND SANITIZER- alcohol gel

Hand Sanitizer by

Drug Labeling and Warnings

Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by ZHEJIANG JINGHUI COSMETICS SHARE CO.,LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

This is a hand sanitizer manufactured according to the Temporary Policy for Preparation of Certain Alcohol-Based Hand Sanitizer Products During the Public Health Emergency (CoViD-19); Guidance for Industry.

The hand sanitizer is manufactured using only the following United States Pharmacopoeia (USP) grade ingredients in the preparation of the product (percentage in final product formulation) consistent with World Health Organization (WHO) recommendations:

1. Alcohol (ethanol) (USP or Food Chemical Codex (FCC) grade) (80%, volume/volume (v/v)) in an aqueous solution denatured according to Alcohol and Tobacco Tax and Trade Bureau regulations in 27 CFR part 20.
2. Glycerol (1.45% v/v).
3. Hydrogen peroxide (0.125% v/v).
4. Sterile distilled water or boiled cold water.

The firm does not add other active or inactive ingredients. Different or additional ingredients may impact the quality and potency of the product.

Active Ingredient(s)

Alcohol 80% v/v. Purpose: Antiseptic

Purpose

Antiseptic, Hand Sanitizer

Use

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

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.

STOP USE

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

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 (59-86F)
• Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

glycerin, hydrogen peroxide, purified water USP

Package Label - Principal Display Panel

60mL NDC: 73905-005-08

INGREDIENTS AND APPEARANCE

HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73905-005
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	80 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
GLYCERIN (UNII: PDC6A3C0OX)
BUTYL ACRYLATE (UNII: 705NM8U35V)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73905-005-01	2 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
2	NDC: 73905-005-02	5 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
3	NDC: 73905-005-03	10 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
4	NDC: 73905-005-04	20 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
5	NDC: 73905-005-05	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
6	NDC: 73905-005-06	45 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
7	NDC: 73905-005-07	55 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
8	NDC: 73905-005-08	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
9	NDC: 73905-005-09	80 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
10	NDC: 73905-005-10	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
11	NDC: 73905-005-11	120 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
12	NDC: 73905-005-12	180 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
13	NDC: 73905-005-13	200 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
14	NDC: 73905-005-14	236 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
15	NDC: 73905-005-15	237 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
16	NDC: 73905-005-16	240 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
17	NDC: 73905-005-17	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
18	NDC: 73905-005-18	260 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
19	NDC: 73905-005-19	300 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
20	NDC: 73905-005-20	350 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
21	NDC: 73905-005-21	400 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
22	NDC: 73905-005-22	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
23	NDC: 73905-005-23	560 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
24	NDC: 73905-005-24	600 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
25	NDC: 73905-005-25	750 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
26	NDC: 73905-005-26	900 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
27	NDC: 73905-005-27	980 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
28	NDC: 73905-005-28	985 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
29	NDC: 73905-005-29	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
30	NDC: 73905-005-30	1300 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
31	NDC: 73905-005-31	1500 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
32	NDC: 73905-005-32	1800 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
33	NDC: 73905-005-33	2000 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
34	NDC: 73905-005-34	2500 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
35	NDC: 73905-005-35	3000 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
36	NDC: 73905-005-36	3800 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
37	NDC: 73905-005-37	4000 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
38	NDC: 73905-005-38	5000 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
39	NDC: 73905-005-39	10000 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
40	NDC: 73905-005-40	20000 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
41	NDC: 73905-005-41	25000 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
42	NDC: 73905-005-42	45000 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
43	NDC: 73905-005-43	50000 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
44	NDC: 73905-005-44	100000 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
45	NDC: 73905-005-45	200000 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
46	NDC: 73905-005-46	500000 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020
47	NDC: 73905-005-47	1000000 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/30/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/30/2020

Labeler - ZHEJIANG JINGHUI COSMETICS SHARE CO.,LTD (529558167)

Establishment
Name	Address	ID/FEI	Business Operations
ZHEJIANG JINGHUI COSMETICS SHARE CO.,LTD		529558167	manufacture(73905-005)