HANDOUT PROTECTION HAND SANITIZER- isopropyl alcohol liquid liquid

HANDOUT PROTECTION HAND SANITIZER by

Drug Labeling and Warnings

HANDOUT PROTECTION HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by ZHEJIANG SAIRUI MEDICAL TECHNOLOGY CO., LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Isoproply Alcohol 75% v/v………………Antiseptic

KEEP OUT OF REACH OF CHILDREN

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

DO NOT USE

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

WARNINGS

For external use only. Flammable. Keep away from heat or flame.

PURPOSE

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

WHEN USING

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

DOSAGE & ADMINISTRATION

Place product on hands to cover all surfaces. Rub hands together untill dry.

• Supervise children under 6 years of age when using this product to avoid swallowing.

INACTIVE INGREDIENT

aloe gel, condensed green tea, glycerine, hydrogen peroxide

STOP USE

If irritation or rash occurs. They may be signs of a serious condition.

INDICATIONS & USAGE

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HANDOUT PROTECTION HAND SANITIZER 
isopropyl alcohol liquid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81820-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	75 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
HYDROGEN PEROXIDE (UNII: BBX060AN9V)
GLYCERIN (UNII: PDC6A3C0OX)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)

Product Characteristics
Color	white (Transparent)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81820-001-01	1 mL in 1 POUCH; Type 0: Not a Combination Product	03/26/2021
2	NDC: 81820-001-02	2 mL in 1 POUCH; Type 0: Not a Combination Product	03/26/2021
3	NDC: 81820-001-03	3 mL in 1 POUCH; Type 0: Not a Combination Product	03/26/2021
4	NDC: 81820-001-04	4 mL in 1 POUCH; Type 0: Not a Combination Product	03/26/2021
5	NDC: 81820-001-05	5 mL in 1 POUCH; Type 0: Not a Combination Product	03/26/2021
6	NDC: 81820-001-06	6 mL in 1 POUCH; Type 0: Not a Combination Product	03/26/2021
7	NDC: 81820-001-07	7 mL in 1 POUCH; Type 0: Not a Combination Product	03/26/2021
8	NDC: 81820-001-08	8 mL in 1 POUCH; Type 0: Not a Combination Product	03/26/2021
9	NDC: 81820-001-09	9 mL in 1 POUCH; Type 0: Not a Combination Product	03/26/2021
10	NDC: 81820-001-10	10 mL in 1 POUCH; Type 0: Not a Combination Product	03/26/2021
11	NDC: 81820-001-11	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/26/2021
12	NDC: 81820-001-12	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/26/2021
13	NDC: 81820-001-13	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/26/2021
14	NDC: 81820-001-14	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/26/2021
15	NDC: 81820-001-15	150 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/26/2021
16	NDC: 81820-001-16	180 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/26/2021
17	NDC: 81820-001-17	200 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/26/2021
18	NDC: 81820-001-18	236 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/26/2021
19	NDC: 81820-001-19	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/26/2021
20	NDC: 81820-001-20	300 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/26/2021
21	NDC: 81820-001-21	350 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/26/2021
22	NDC: 81820-001-22	400 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/26/2021
23	NDC: 81820-001-23	450 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/26/2021
24	NDC: 81820-001-24	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/26/2021
25	NDC: 81820-001-25	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/26/2021
26	NDC: 81820-001-26	2000 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/26/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/26/2021

Labeler - ZHEJIANG SAIRUI MEDICAL TECHNOLOGY CO., LTD. (554552501)

Establishment
Name	Address	ID/FEI	Business Operations
ZHEJIANG SAIRUI MEDICAL TECHNOLOGY CO., LTD.		554552501	manufacture(81820-001)