Skin delight Hand WashGel by INTERKOS CO., LTD. Drug Facts

Drug Details [pdf]

SKIN DELIGHT HAND WASHGEL- alcohol gel
INTERKOS CO., LTD.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Drug Facts

alcohol

Water
Carbomer
Triethanolamine
PEG-60 Hydrogenated Castor Oil
Fragrance
Chlorphenesin
Trideceth-10
Butylene Glycol
Salix Alba (Willow) Bark Extract
Origanum Vulgare Leaf Extract
Chamaecyparis Obtusa Leaf Extract
Portulaca Oleracea Extract
Lactobacillus/Soybean Ferment Extract
Cinnamomum Cassia Bark Extract
Scutellaria Baicalensis Root Extract
Vincetoxicum Atratum Extract
1,2-Hexanediol
Caprylyl Glycol
Aloe Barbadensis Leaf Extract
Illicium Verum (Anise) Fruit Extract

Protecting hands from the harmful environment and keeping hands healthy and clean with feeling sense the freshness without stinckness.

KEEP OUT OF REACH OF THE CHILDREN

Share some portion onto the palm and evenly spread it.

1. If any one of following symptoms occurs when using cosmetics, stop using it and consult a dermatologist.
A.red spot. swelling, itching, stimulus.
B.symptoms mentioned above are caused by sunlight.
2. Do not apply on skin where there is wound, eczema, or irritation.
3. Do not use for the purpose other than indicated.
4. Storage and cautions for handling.
A. keep out of reach of children.
B.keep away from direct sunlight.

for external use only

label label

SKIN DELIGHT HAND WASHGEL
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77049-0006
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	61.75 mL in 100 mL

Ingredient Name	Strength
Inactive Ingredients
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CARBOMER 940 (UNII: 4Q93RCW27E)
TROLAMINE (UNII: 9O3K93S3TK)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
WATER (UNII: 059QF0KO0R)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC: 77049-0006-1	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/23/2020	03/01/2021

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	10/23/2020	03/01/2021

Labeler - INTERKOS CO., LTD. (689850314)

Registrant - INTERKOS CO., LTD. (689850314)

Name	Address	ID/FEI	Business Operations
Establishment
INTERKOS CO., LTD.		689850314	manufacture(77049-0006)

Revised: 11/2021

Document Id: 51b37d85-7d5b-4326-a1e9-f1af9c0451de

Set id: b25007b5-ee18-02fa-e053-2a95a90aad7d

Version: 2

Effective Time: 20211122