75% ALCOHOL DISINFECTANT- alcohol liquid

75% Alcohol Disinfectant by

Drug Labeling and Warnings

75% Alcohol Disinfectant by is a Otc medication manufactured, distributed, or labeled by Zhongrong Technology Corporation Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Ethyl Alcohol 75% v/v. Purpose: Disinfection

Purpose

Disinfection, 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 and flame, Keep out of reach of children.

Avoid contact with face, eyes and broken skin. If irritation occurs, seek medical advice.

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

purified water

Package Label - Principal Display Panel

2500 mL NDC: 81191-001-15

INGREDIENTS AND APPEARANCE

75% ALCOHOL DISINFECTANT 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81191-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	75 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81191-001-01	30 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	11/26/2020
2	NDC: 81191-001-02	50 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	11/26/2020
3	NDC: 81191-001-03	60 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	11/26/2020
4	NDC: 81191-001-04	100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	11/26/2020
5	NDC: 81191-001-05	150 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	11/26/2020
6	NDC: 81191-001-06	200 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	11/26/2020
7	NDC: 81191-001-07	236 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	11/26/2020
8	NDC: 81191-001-08	240 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	11/26/2020
9	NDC: 81191-001-09	300 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	11/26/2020
10	NDC: 81191-001-10	500 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	11/26/2020
11	NDC: 81191-001-11	600 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	11/26/2020
12	NDC: 81191-001-12	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/26/2020
13	NDC: 81191-001-13	1500 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/26/2020
14	NDC: 81191-001-14	2000 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/26/2020
15	NDC: 81191-001-15	2500 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/26/2020
16	NDC: 81191-001-16	3000 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/26/2020
17	NDC: 81191-001-17	3780 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/26/2020
18	NDC: 81191-001-18	5000 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/26/2020
19	NDC: 81191-001-19	200000 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/26/2020
20	NDC: 81191-001-20	1000000 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/26/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	11/25/2020

Labeler - Zhongrong Technology Corporation Ltd. (529575698)

Registrant - Zhongrong Technology Corporation Ltd. (529575698)

Establishment
Name	Address	ID/FEI	Business Operations
Zhongrong Technology Corporation Ltd.		529575698	manufacture(81191-001) , label(81191-001)