Drug Facts

Active ingredient

Ethyl Alcohol 62.0%

Purpose

Antimicrobial

Keep out of reach of children.Children must be supervised in use of this product.

For external use only.
Flammable.Keep away from fire or flame.
Do not apply around eyes.Do not use in ears & mouth.
When using this product, avoid contact with eyes. In case of contact flush eyes with water.
Stop use and ask a doctor if redness or irritation develop and persist for more than 72 hours.

Water, Trolamine,Glycerin, carbormer,Tocopherol Acetate, Aloe Vera.

NDC:70675-001-01

10ML

NDC:70675-001-02

15ML

NDC:70675-001-03

20ML

NDC:70675-001-04

30ML

NDC:70675-001-05

50ML

NDC:70675-001-06

60ML

NDC:70675-001-07

100ML

NDC:70675-001-08

120ML

NDC:70675-001-09

240ML

NDC:70675-001-10

500ML

HAND SANITIZER
alcohol liquid

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 mL in 100 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
TROLAMINE (UNII: 9O3K93S3TK)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:70675-001-01	10 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/27/2023
2	NDC:70675-001-02	15 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/27/2023
3	NDC:70675-001-03	20 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/27/2023
4	NDC:70675-001-04	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/27/2023
5	NDC:70675-001-05	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/27/2023
6	NDC:70675-001-06	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/27/2023
7	NDC:70675-001-07	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/27/2023
8	NDC:70675-001-08	120 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/27/2023
9	NDC:70675-001-09	240 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/27/2023
10	NDC:70675-001-10	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/27/2023

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	505G(a)(3)	11/27/2023

Labeler - Deqing Jiarou Daily Chemical Co., Ltd (544398724)

Registrant - Deqing Jiarou Daily Chemical Co., Ltd (544398724)

Name	Address	ID/FEI	Business Operations
Establishment
Deqing Jiarou Daily Chemical Co., Ltd		544398724	manufacture(70675-001)