Active Ingredients

Ethyl Alcohol 75%

Purpose

Uses

Hand Sanitizer to help reduce bacteria on skin.

Warnings

For external use only.Keep out of reach of children.Children must be supervised if using this product.

Flammable.Keep away from fire or flame.

Avoid contact with eyes.Discontinue use if irritation or redness occurs.If irritation continues for more than 72hrs, please

consult a doctor.

Directions

Place enough in your palm to thoroughly spread on both and rub into the skin until dry.

Children under 6 years of age should be supervised when using this product.

Other Information

store below 160°F.(41℃)

may discolor certain fabrics or surfaces

Inactive Ingredients

Water(Aqua),Carbomer, Glycerol,Propylene Glycol,triethanolamine,Poly(acrylic acid)

Package Label - Principal Display Panel

74046-001-17 80ml 74046-001-12 10ml 74046-001-18 120ml 74046-001-16 70ml 74046-001-20 450ml 74046-001-19 300ml 74046-001-11 3ml 74046-001-14 38ml 74046-001-13 20ml 74046-001-15 45ml 15 ml label 30 ml label 40 ml label 50 ml label 60 ml label 100 ml label 236 ml label 240 ml label 250 ml label 500 ml label

HAND SANITIZER GEL
hand sanitizer gel gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:74046-001
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	75 mL in 100 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
TROLAMINE (UNII: 9O3K93S3TK)
ACRYLIC ACID (UNII: J94PBK7X8S)
GLYCERIN (UNII: PDC6A3C0OX)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:74046-001-01	15 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/14/2020
2	NDC:74046-001-02	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/14/2020
3	NDC:74046-001-03	40 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/14/2020
4	NDC:74046-001-04	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/14/2020
5	NDC:74046-001-05	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/14/2020
6	NDC:74046-001-06	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/14/2020
7	NDC:74046-001-07	236 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/14/2020
8	NDC:74046-001-08	240 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/14/2020
9	NDC:74046-001-09	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/14/2020
10	NDC:74046-001-10	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/14/2020
11	NDC:74046-001-17	80 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/14/2020
12	NDC:74046-001-11	3 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/14/2020
13	NDC:74046-001-12	10 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/14/2020
14	NDC:74046-001-13	20 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/14/2020
15	NDC:74046-001-18	120 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/14/2020
16	NDC:74046-001-19	300 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/14/2020
17	NDC:74046-001-14	38 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/14/2020
18	NDC:74046-001-15	45 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/14/2020
19	NDC:74046-001-20	450 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/14/2020
20	NDC:74046-001-16	70 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/14/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	04/14/2020

Labeler - Dongguan Mingyi Medical Products Co., Ltd. (554526907)

Registrant - Dongguan Mingyi Medical Products Co., Ltd. (554526907)

Name	Address	ID/FEI	Business Operations
Establishment
Dongguan Mingyi Medical Products Co., Ltd.		554526907	manufacture(74046-001)

74046-001 Hand Sanitizer Gel