INSTANT HAND SANITIZER gel

Instant Hand Sanitizer by

Drug Labeling and Warnings

Instant Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Guangzhou Yucaitang Cosmetics Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Alcohol 75%(v/v)

Purpose

Antimicrobial

Uses

Hand Sanitizer to help reduce bacteria on skin.

WARNINGS

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

only.

DO NOT USE

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.

STOP USE

KEEP OUT OF REACH OF CHILDREN

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 below 106°F.(4I°C)

May discolor certain fabrics or surfaces

INACTIVE INGREDIENTS

WATER,GLYCERIN,CARBOMER,AMINOMETHYL PROPANOL

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

INSTANT HAND SANITIZER 
instant hand sanitizer gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75439-002
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
GLYCERIN (UNII: PDC6A3C0OX)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75439-002-01	5 mL in 1 BAG; Type 0: Not a Combination Product	05/14/2020
2	NDC: 75439-002-02	29 mL in 1 AMPULE; Type 0: Not a Combination Product	05/14/2020
3	NDC: 75439-002-03	30 mL in 1 AMPULE; Type 0: Not a Combination Product	05/14/2020
4	NDC: 75439-002-04	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/14/2020
5	NDC: 75439-002-05	59 mL in 1 AMPULE; Type 0: Not a Combination Product	05/14/2020
6	NDC: 75439-002-06	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/14/2020
7	NDC: 75439-002-07	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/14/2020
8	NDC: 75439-002-08	200 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/14/2020
9	NDC: 75439-002-09	238 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/14/2020
10	NDC: 75439-002-10	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/14/2020
11	NDC: 75439-002-11	260 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/14/2020
12	NDC: 75439-002-12	300 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/14/2020
13	NDC: 75439-002-13	400 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/14/2020
14	NDC: 75439-002-14	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/14/2020
15	NDC: 75439-002-15	750 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/14/2020
16	NDC: 75439-002-16	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/14/2020
17	NDC: 75439-002-17	1250 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/14/2020
18	NDC: 75439-002-18	2000 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/14/2020
19	NDC: 75439-002-19	5000 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/14/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/14/2020

Labeler - Guangzhou Yucaitang Cosmetics Co., Ltd (526897391)

Registrant - Guangzhou Yucaitang Cosmetics Co., Ltd (526897391)

Establishment
Name	Address	ID/FEI	Business Operations
Guangzhou Yucaitang Cosmetics Co., Ltd		526897391	manufacture(75439-002)