HANDOUT PROTECTION HAND SANITIZER- isopropyl alcohol liquid

HANDOUT protection hand sanitizer by

Drug Labeling and Warnings

HANDOUT protection hand sanitizer by is a Otc medication manufactured, distributed, or labeled by KINGKEY MBC LIFE TECHNOLOGY GROUP CO., LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

lsopropyl Alcohol 75% v/v

Purpose

Antiseptic

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

WHEN USING

When using this productkeep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor ifirritation 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.

Do not use
In children less than 2 months of age
On open skin wounds

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

Do not store above 105F

Inactive ingredients

aloe gel, condensed green tea, glycerin, Hydrogen peroxide

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

HANDOUT PROTECTION HAND SANITIZER 
isopropyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73928-012
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
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERIN (UNII: PDC6A3C0OX)
HYDROGEN PEROXIDE (UNII: BBX060AN9V)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73928-012-01	1 mL in 1 POUCH; Type 0: Not a Combination Product	09/28/2020
2	NDC: 73928-012-02	2 mL in 1 POUCH; Type 0: Not a Combination Product	09/28/2020
3	NDC: 73928-012-03	3 mL in 1 POUCH; Type 0: Not a Combination Product	09/28/2020
4	NDC: 73928-012-04	4 mL in 1 POUCH; Type 0: Not a Combination Product	09/28/2020
5	NDC: 73928-012-05	5 mL in 1 POUCH; Type 0: Not a Combination Product	09/28/2020
6	NDC: 73928-012-06	6 mL in 1 POUCH; Type 0: Not a Combination Product	09/28/2020
7	NDC: 73928-012-07	7 mL in 1 POUCH; Type 0: Not a Combination Product	09/28/2020
8	NDC: 73928-012-08	8 mL in 1 POUCH; Type 0: Not a Combination Product	09/28/2020
9	NDC: 73928-012-09	9 mL in 1 POUCH; Type 0: Not a Combination Product	09/28/2020
10	NDC: 73928-012-10	10 mL in 1 POUCH; Type 0: Not a Combination Product	09/28/2020
11	NDC: 73928-012-11	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/28/2020
12	NDC: 73928-012-12	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/28/2020
13	NDC: 73928-012-13	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/28/2020
14	NDC: 73928-012-14	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/28/2020
15	NDC: 73928-012-15	150 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/28/2020
16	NDC: 73928-012-16	180 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/28/2020
17	NDC: 73928-012-17	200 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/28/2020
18	NDC: 73928-012-18	236 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/28/2020
19	NDC: 73928-012-19	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/28/2020
20	NDC: 73928-012-20	300 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/28/2020
21	NDC: 73928-012-21	350 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/28/2020
22	NDC: 73928-012-22	400 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/28/2020
23	NDC: 73928-012-23	450 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/28/2020
24	NDC: 73928-012-24	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/28/2020
25	NDC: 73928-012-25	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/28/2020
26	NDC: 73928-012-26	2000 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/28/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	09/28/2020

Labeler - KINGKEY MBC LIFE TECHNOLOGY GROUP CO., LTD (545349263)

Establishment
Name	Address	ID/FEI	Business Operations
KINGKEY MBC LIFE TECHNOLOGY GROUP CO., LTD		545349263	manufacture(73928-012)