OTC Medication Information: Black Snail Collagen Serum

BLACK SNAIL COLLAGEN SERUM- snail, unspecified liquid
NOKSIBCHO cosmetic Co., Ltd.

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Snail Secretion Filtrate

Water
Glycerin
Propylene Glycol
Alcohol
1,2-Hexanediol
Glycerin
Glyceryl Acrylate/Acrylic Acid Copolymer
Propylene Glycol
PVM/MA Copolymer
PEG/PPG-18/4 Copolymer
Betaine
Allantoin
Adenosine
Butylene glycol
Carbomer
Aloe Barbadensis Leaf Extract
Hydrolyzed Collagen
Copper Tripeptide-1
Black Soybean Extract
Sesamum Indicum (Sesame)
Seed Extract
Oryza Sativa (Rice) Extract
Panax Ginseng Berry Extract
Leontopodium alpinum extract
Buddleja Davidii Extract
Malva Sylvestris (Mallow) Flower Extract
Theobroma Cacao (Cocoa) Extract
PEG-60 Hydrogenated Castor Oil
Arginine
Phenoxyethanol
Ethylhexylglycerin
Parfum

anti-wrinkle and nourish

keep out of reach of the children

apply proper amount and gently massage

For external use only When using this product

■ if the following 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
(click image for full-size original)

BLACK SNAIL COLLAGEN SERUM snail secretion filtrate, collagen liquid
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:73590-0013
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SNAIL, UNSPECIFIED (SNAIL, UNSPECIFIED) SNAIL, UNSPECIFIED 60 g in 100 mL
Inactive Ingredients
Ingredient Name Strength
WATER
BUTYLENE GLYCOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:73590-0013-1 50 mL in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved drug other 03/14/2020
Labeler — NOKSIBCHO cosmetic Co., Ltd. (690182175)
Registrant — NOKSIBCHO cosmetic Co., Ltd. (690182175)
Establishment
Name Address ID/FEI Operations
NOKSIBCHO cosmetic Co., Ltd. 690182175 manufacture (73590-0013)

Revised: 03/2020 NOKSIBCHO cosmetic Co., Ltd.

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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