AIR RAID CARD WATERLESS ALCOHOL HAND SANITIZER GEL- waterless alcohol hand sanitizer gel gel

Air raid card Waterless Alcohol Hand Sanitizer Gel by

Drug Labeling and Warnings

Air raid card Waterless Alcohol Hand Sanitizer Gel by is a Otc medication manufactured, distributed, or labeled by Jiangsu Manwei Pharmaceutical Co.,Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethanol 75%(V/V)

Purpose

Disinfectant

Uses

Can kill bacteria on hands suchas: Escherichia coli, Staphylococcus aureusCandida albicans

Warnings

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

When using this product

When using this product]do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water Stop use and ask doctor if irritation or rash appears and lasts. Keep out of reach for children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• Place enough Product in your palm to thoroughly spread on both hands and rub into the skin until dry
• Children under 6 years of age should be supervised when using this product

Other information

Store in a cool and ventilated place under 22 C

Inactive ingredients

Weter Carbomer Triethanolamine

STOP USE

DO NOT USE

KEEP OUT OF REACH OF CHILDREN

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

AIR RAID CARD WATERLESS ALCOHOL HAND SANITIZER GEL 
waterless alcohol hand sanitizer gel gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75086-119
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
CARBOMER 934 (UNII: Z135WT9208)
TROLAMINE (UNII: 9O3K93S3TK)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75086-119-01	8 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/20/2020
2	NDC: 75086-119-02	10 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/20/2020
3	NDC: 75086-119-03	15 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/20/2020
4	NDC: 75086-119-04	20 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/20/2020
5	NDC: 75086-119-05	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/20/2020
6	NDC: 75086-119-06	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/20/2020
7	NDC: 75086-119-07	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/20/2020
8	NDC: 75086-119-08	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/20/2020
9	NDC: 75086-119-09	300 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/20/2020
10	NDC: 75086-119-10	350 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/20/2020
11	NDC: 75086-119-11	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/20/2020
12	NDC: 75086-119-12	3800 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/20/2020
13	NDC: 75086-119-13	5000 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/20/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/20/2020

Labeler - Jiangsu Manwei Pharmaceutical Co.,Ltd (554529430)

Establishment
Name	Address	ID/FEI	Business Operations
Jiangsu Manwei Pharmaceutical Co.,Ltd		554529430	manufacture(75086-119)