TAEYANGSOO PLAVITAL EYE ALLCream: Package Insert and Label Information

TAEYANGSOO PLAVITAL EYE ALLCREAM- niacinamide and adenosine liquid
Unimed Pharmaceuticals, Inc.

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.

adenosine, niacinamide

Camellia Sinensis Leaf Water, Hydrolyzed Placental Extract(12.5%),
Glycerin, Butylene Glycol, Cocos Nucifera (Coconut) Oil, Sodium
Hyaluronate, Persea Gratissima (Avocado) Oil, Vinyl Dimethicone,
1,2-Hexanediol, Hydrolyzed Collagen, Cetearyl Olivate, Sorbitan
Olivate, Cetearyl Alcohol, Polyglyceryl-3 Methylglucose Distearate,
Beeswax, Butyrospermum Parkii (Shea) Butter, Dipentaerythrityl
Hexahydroxystearate/Hexastearate/Hexarosinate, Sodium Acrylate/
Sodium Acryloyldimethyl Taurate Copolymer, Betaine, Water, Fragran
ce, Isohexadecane, Acrylates/C10-30 Alkyl Acrylate Crosspolymer,
Trehalose, Tromethamine, Hydroxyethyl Acrylate/Sodium Acryloyl
dimethyl Taurate Copolymer, Limonene, Panthenol, Sasa Quelpaer
tensis Extract, Centella Asiatica Extract, Polygonum Cuspidatum
Root Extract, Scutellaria Baicalensis Root Extract, Camellia Sinensis
Leaf Extract, Glycyrrhiza Glabra (Licorice) Root Extract, Anthemis No
bilis Flower Extract, Rosmarinus Officinalis (Rosemary) Leaf Extract,
Polysorbate 80, Allantoin, Ethylhexylglycerin, Adenosine, Sorbitan
Oleate, Disodium EDTA, Citral, Butylphenyl Methylpropional, Linalo
ol, Glutathione

Skin brightening, Anti wrinkle

keep out of reach of the children

Softly apply cream along the skin and pat gently for better absorption

1. For external use only
2. Avoid contact with eyes. In case of contact with eyes, rinse imme
diately with water
3. Do not use the product on an open skin wound or on areas of eczema or infection

external use only

(click image for full-size original)

TAEYANGSOO PLAVITAL EYE ALLCREAM adenosine, niacinamide liquid
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:73669-007
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Inactive Ingredients
Ingredient Name Strength
# Item Code Package Description Multilevel Packaging
1 NDC:73669-007-01 50 mL in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved drug other 04/04/2021
Labeler — Unimed Pharmaceuticals, Inc. (689852052)
Registrant — Unimed Pharmaceuticals, Inc. (689852052)
Name Address ID/FEI Operations
Unimed Pharmaceuticals, Inc. 689852052 label (73669-007)
Name Address ID/FEI Operations
C&t Dream Co., Ltd 694699750 manufacture (73669-007)

Revised: 04/2021 Unimed Pharmaceuticals, Inc.

DrugInserts.com provides trustworthy package insert and label information about marketed drugs as submitted by manufacturers to the US Food and Drug Administration. Package information is not reviewed or updated separately by DrugInserts.com. Every individual package label entry contains a unique identifier which can be used to secure further details directly from the US National Institutes of Health and/or the FDA.

As the leading independent provider of trustworthy medication information, we source our database directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. Our material is not intended as a substitute for direct consultation with a qualified health professional.

Terms of Use | Copyright © 2021. All Rights Reserved.