G9 SKIN AC SOLUTIONCLEANSER by COSMELAB Co., Ltd. / Nowcos.Co.,Ltd Drug Facts

Drug Details [pdf]

G9 SKIN AC SOLUTIONCLEANSER- salicylic acid liquid
COSMELAB 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.

----------

Drug Facts

salicylic acid

Water, Glycerin, Palmitic Acid, Stearic Acid, Lauric Acid, Myristic Acid, Potassium Hydroxide, Glyceryl Stearate SE, Cocamide DEA, Propylene Glycol, Beeswax, Cocamidopropyl Betaine, Glycol Distearate, PEG-60 Hydrogenated Castor Oil, Phenoxyethanol, Fragrance, Sodium Chloride, Chlorphenesin, Centella Asiatica Extract, Tocopheryl Acetate, Alcohol, Disodium EDTA, BHT, Butylene Glycol, Eucalyptus Globulus Leaf Extract, Sophora Angustifolia Root Extract, 1,2-Hexanediol, Hamamelis Virginiana (Witch Hazel) Extract, Citrus Paradisi (Grapefruit) Fruit Extract

for Sensitive and troubled skin, specially ACNE skin type care

keep out of reach of the children

■ following the use of base, take a suitable amount on the back of your hand and apply it over your face thinly following skin texture

■ gently rub with your fingers as like doing massage and wash off the remains

■ if following abnormal symptoms occurs after use , stop use and consult with a skin specialist

red specks, swelling, itching

■ don’t use on the part where there is injury, eczema, or dermatitis

Keep out of reach of children

■ if swallowed, get medical help or contact a person control center immediately

for external use only

label

G9 SKIN AC SOLUTIONCLEANSER
salicylic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71790-002
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	0.5 g in 100 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC: 71790-002-01	120 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/01/2019	12/13/2019

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part333D	03/01/2019	12/13/2019

Labeler - COSMELAB Co., Ltd. (688211711)

Registrant - COSMELAB Co., Ltd. (688211711)

Name	Address	ID/FEI	Business Operations
Establishment
COSMELAB Co., Ltd.		688211711	label(71790-002)

Name	Address	ID/FEI	Business Operations
Establishment
Nowcos.Co.,Ltd		689914984	manufacture(71790-002)

Revised: 12/2019

Document Id: 999166de-5f84-6c99-e053-2995a90adf0b

Set id: 82fe6ba1-3aa2-f9ee-e053-2991aa0a2e9a

Version: 2

Effective Time: 20191213