U INSTANT HAND SANITIZER CLASSIC- alcohol solution

U Instant Hand Sanitizer Classic by

Drug Labeling and Warnings

U Instant Hand Sanitizer Classic by is a Otc medication manufactured, distributed, or labeled by Zhejiang Shenying Technology Co., Ltd. Jiaojiang Branch. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Ethyl Alcohol 70%

Purpose

Antimicrobial

Use

Hand sanitizer to help reduce bacteria on the skin

Warnings

For external use only

Flammable. Keep away from fire or flame

WHEN USING

When using this product do not use in or near eyes. In case of eye contact, rinse eyes thoroughly with water.

STOP USE

Stop use and ask a doctor if irritation or rash appears and lasts

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 in your palm to thoroughly spread on both hands and rub into skin  untill dry

Children under six years of age should be supervised when using this product

Other information

Store below 106F (41C)

May discolor certain fabrics or surfaces

Inactive ingredients

Water, aloe barbadensis leaf jiuce, carbomer, fragrance, glycerin, propylene glycol, triethanolamine, tocopheryl acetate, 2-(dimethylamino) ethanol

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

U INSTANT HAND SANITIZER CLASSIC 
alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75112-006
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
CARBOMER 940 (UNII: 4Q93RCW27E)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
TROLAMINE (UNII: 9O3K93S3TK)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75112-006-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/14/2020
2	NDC: 75112-006-02	54 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/14/2020
3	NDC: 75112-006-03	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/14/2020
4	NDC: 75112-006-04	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/14/2020
5	NDC: 75112-006-05	237 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/14/2020
6	NDC: 75112-006-06	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/14/2020
7	NDC: 75112-006-07	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/14/2020
8	NDC: 75112-006-08	1800 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/14/2020
9	NDC: 75112-006-09	3780 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/14/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	08/14/2020

Labeler - Zhejiang Shenying Technology Co., Ltd. Jiaojiang Branch (414137820)

Registrant - Zhejiang Shenying Technology Co., Ltd. Jiaojiang Branch (414137820)

Establishment
Name	Address	ID/FEI	Business Operations
Zhejiang Shenying Technology Co., Ltd. Jiaojiang Branch		414137820	manufacture(75112-006)