ALCOHOL HAND SANITIZER GEL- alcohol gel

Alcohol Hand Sanitizer Gel by

Drug Labeling and Warnings

Alcohol Hand Sanitizer Gel by is a Otc medication manufactured, distributed, or labeled by Shantou Kangjie Daily Chemical Industry Co.,Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethyl Alcohol 75%

Purpose

Antimicrobial

Uses

Hand Sanitizer to help reduce bacteria on skin.

WARNINGS

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

DO NOT USE

WHEN USING

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.(41℃)

May discolor certain fabrics or surfaces.

INACTIVE INGREDIENTS

Water(Aqua) ,Aloe Barbadensis Leaf Juice,Carbomer,Fragrance,Glycerin,Propylene Glycol,Tocopheryl

Acetate(Vitamin E) ,Triethanolamine, FD&C Blue No.1,FD&C Yellow No 5.

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

ALCOHOL HAND SANITIZER GEL 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74047-001
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
GLYCERIN (UNII: PDC6A3C0OX)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
TROLAMINE (UNII: 9O3K93S3TK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74047-001-01	20 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/16/2020
2	NDC: 74047-001-02	25 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/16/2020
3	NDC: 74047-001-03	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/16/2020
4	NDC: 74047-001-04	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/16/2020
5	NDC: 74047-001-05	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/16/2020
6	NDC: 74047-001-06	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/16/2020
7	NDC: 74047-001-07	120 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/16/2020
8	NDC: 74047-001-08	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/16/2020
9	NDC: 74047-001-09	300 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/16/2020
10	NDC: 74047-001-10	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/16/2020
11	NDC: 74047-001-11	800 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/16/2020
12	NDC: 74047-001-12	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/16/2020
13	NDC: 74047-001-13	4000 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/16/2020
14	NDC: 74047-001-14	5000 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/16/2020
15	NDC: 74047-001-15	25000 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/16/2020
16	NDC: 74047-001-16	50000 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/16/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/16/2020

Labeler - Shantou Kangjie Daily Chemical Industry Co.,Ltd (527128712)

Registrant - Shantou Kangjie Daily Chemical Industry Co.,Ltd (527128712)

Establishment
Name	Address	ID/FEI	Business Operations
Shantou Kangjie Daily Chemical Industry Co.,Ltd		527128712	manufacture(74047-001)