NON-WASH DISINFECTANT- alcohol liquid NON-WASH SANITISERGEL- alcohol liquid

Non-Wash SanitiserGel by

Drug Labeling and Warnings

Non-Wash SanitiserGel by is a Otc medication manufactured, distributed, or labeled by Shera Heman Zhejiang Biotechnologies Co.,Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Non-wash Disinfectant;
Non-wash Sanitiser Gel

Active Ingredient(s)

Alcohol 75% v/v. Purpose: Antiseptic

Purpose

Antiseptic

Use

Non-wash Disinfectant, Non-wash Sanitiser Gel 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

Non-wash Disinfectant:

purified water USP

Non-wash Sanitiser Gel:

WATER
CARBOMER
GLYCERIN

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

NON-WASH DISINFECTANT 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74457-101
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: 74457-101-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/24/2020
2	NDC: 74457-101-02	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/24/2020
3	NDC: 74457-101-03	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/24/2020
4	NDC: 74457-101-04	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/24/2020
5	NDC: 74457-101-05	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/24/2020
6	NDC: 74457-101-06	300 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/24/2020
7	NDC: 74457-101-07	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/24/2020
8	NDC: 74457-101-08	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/24/2020
9	NDC: 74457-101-09	4000 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/24/2020
10	NDC: 74457-101-10	5000 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/24/2020
11	NDC: 74457-101-11	25000 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/24/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	12/24/2020

NON-WASH SANITISERGEL 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74457-201
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)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74457-201-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/24/2020
2	NDC: 74457-201-02	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/24/2020
3	NDC: 74457-201-03	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/24/2020
4	NDC: 74457-201-04	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/24/2020
5	NDC: 74457-201-05	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/24/2020
6	NDC: 74457-201-06	300 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/24/2020
7	NDC: 74457-201-07	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/24/2020
8	NDC: 74457-201-08	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/24/2020
9	NDC: 74457-201-09	4000 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/24/2020
10	NDC: 74457-201-10	5000 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/24/2020
11	NDC: 74457-201-11	25000 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/24/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	12/24/2020

Labeler - Shera Heman Zhejiang Biotechnologies Co.,Ltd. (554528847)

Establishment
Name	Address	ID/FEI	Business Operations
Shera Heman Zhejiang Biotechnologies Co.,Ltd.		554528847	manufacture(74457-101, 74457-201)