SKINDOM HAND CLEAN- alcohol gel

SKINDOM Hand Clean by

Drug Labeling and Warnings

SKINDOM Hand Clean by is a Otc medication manufactured, distributed, or labeled by THE SUN CO.LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredients: Alcohol 62.0%

INACTIVE INGREDIENT

Inactive ingredients:

Water, Carbomer, Triethanolamine, Propylene Glycol, Aloe Barbadenesis Leaf Extract, Sodium Hyaluronate, Copper Tripeptide-1, Fragrance, Limonene

PURPOSE

PURPOSE: Antimicrobial

WARNINGS

Warnings:

For external use only.

Flammable. Keep away from heat and flame.

DO NOT USE in the eyes. In case of contact, rinse eyes thoroughly with water

Stop use and ask a doctor if skin irritation and redness develop and persist for more than 72 hours.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Uses

Uses

For handwashing to decrease bacteria on the skin, recommended for repeated use

Directions

Directions

- Wet hands thoroughly with product
- Briskly rub hands together until dry
- Supervise children under 6 years in the use of this product

Other Information

Other Information

- Store at 20°C to 25°C (68°F to 77°F)
- May discolor certain fabrics

QUESTIONS

Questions
www.skindom.co.kr

Package Label : SKINDOM Hand Clean Gel 60mL * 4ea

Package Label : SKINDOM Hand Clean Gel 300mL * 2ea

INGREDIENTS AND APPEARANCE

SKINDOM HAND CLEAN 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74923-070
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)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
TROLAMINE (UNII: 9O3K93S3TK)
Propylene Glycol (UNII: 6DC9Q167V3)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
PREZATIDE COPPER (UNII: 6BJQ43T1I9)
LIMONENE, (+)- (UNII: GFD7C86Q1W)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74923-070-02	4 in 1 CARTON	04/01/2020
1	NDC: 74923-070-01	60 mL in 1 CONTAINER; Type 0: Not a Combination Product
2	NDC: 74923-070-04	2 in 1 CARTON	04/01/2020
2	NDC: 74923-070-03	300 mL in 1 CONTAINER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	04/01/2020

Labeler - THE SUN CO.LTD (694433104)

Registrant - THE SUN CO.LTD (694433104)

Establishment
Name	Address	ID/FEI	Business Operations
THE SUN CO.LTD		694433104	manufacture(74923-070)