HAND SANITIZER- alcohol liquid

HAND SANITIZER by

Drug Labeling and Warnings

HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by Deqing Jiarou Daily Chemical Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

Ethyl Alcohol 62.0%

Purpose

Antimicrobial

KEEP OUT OF REACH OF CHILDREN

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

Uses

• Hand sanitizer to help decrease bacteria on the skin.
• When water, soap & towel are not available.
• Recommended for repeated use.

Warning

• 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.

Directions

• Squirt as needed into your palms and thoroughly spread on both hands.
• Rub into skin until dry.

OTHER SAFETY INFORMATION

• Store in original container closed.
• Store at 20°C to 25°C （68°F to 77°F）.
• May discolor fabrics.

Inactive ingredients

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

Packaging

NDC: 70675-001-01

NDC: 70675-001-02

NDC: 70675-001-03

NDC: 70675-001-04

NDC: 70675-001-05

NDC: 70675-001-06

NDC: 70675-001-07

NDC: 70675-001-08

NDC: 70675-001-09

NDC: 70675-001-10

INGREDIENTS AND APPEARANCE

HAND SANITIZER 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70675-001
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
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)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
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 Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
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)

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