SANCARE ANTISEPTIC HAND- alcohol gel

Sancare Antiseptic Hand by

Drug Labeling and Warnings

Sancare Antiseptic Hand by is a Otc medication manufactured, distributed, or labeled by Ester Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredients: ALCOHOL 75%

INACTIVE INGREDIENT

Inactive ingredients:

Water, Aloe Barbadensis Leaf Extract, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Triethanolamine

PURPOSE

Purpose: ANTISEPTIC

WARNINGS

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 a doctor if irritation or redness develops.

Keep our of reach of children. If swallowed get medical help or contact a Poison Control Center right away.

KEEP OUT OF REACH OF CHILDREN

Keep our of reach of children. If swallowed get medical help or contact a Poison Control Center right away.

Uses

Uses:

For handwashing when water is not available to decrease bacteria on the skin
- after changing diapers
- after assisting ill persons
- before contact with a person under medical care or treatment
- recommended for repeated use

Directions

Directions:

- apply palmful to hands
- rub hands together vigorously until dry
- supervise children in the use of this product

PACKAGE LABEL - Sancare Antiseptic Hand Gel 30mL * 20ea Carton

PACKAGE LABEL - Sancare Antiseptic Hand Gel 500mL Bottle

INGREDIENTS AND APPEARANCE

SANCARE ANTISEPTIC HAND 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74004-010
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	75.0 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
TROLAMINE (UNII: 9O3K93S3TK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74004-010-02	20 in 1 CARTON	03/01/2020
1	NDC: 74004-010-01	30 mL in 1 POUCH; Type 0: Not a Combination Product
2	NDC: 74004-010-03	500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	03/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	03/01/2020

Labeler - Ester Co., Ltd. (688425766)

Registrant - Ester Co., Ltd. (688425766)

Establishment
Name	Address	ID/FEI	Business Operations
Ester Co., Ltd.		688425766	manufacture(74004-010)