Label: CONJU PRINCESS LIFTING- adenosine cream
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Contains inactivated NDC Code(s)
NDC Code(s): 72950-060-01, 72950-060-02 - Packager: Conju Korea Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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.
Drug Label Information
Updated March 15, 2019
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- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Inactive ingredients:
Water, Dipropylene Glycol, Glycerin, PEG-240/HDI copolymer BIS-decyltetradeceth-20 Ether, Cetyl Ethylhexanoate, 1,2-Hexanediol, Glycosyl Trehalose, Hydrogenated Starch Hydrolysate, PEG-100 Stearate, Macadamia Ternifolia Seed Oil, Caprylic/Capric Triglyceride, Olea Europaea (Olive) Fruit Oil, Glyceryl Stearate, PEG-100 Stearate, Allantoin, Dipotassium Glycyrrhizate, Disodium EDTA, Tocopheryl Acetate, Pelargonium Graveolens Flower Oil, Eucalyptus Globulus Leaf Oil, Rosmarinus Officinalis (Rosemary) Leaf Oil, Anthemis Nobilis Flower Oil, Polyepsilon-Lysine, Sodium Hyaluronate, Centella Asiatica Leaf Extract, Vitis Vinifera (Grape) Callus Culture Extract, Ethylhexylglycerin, Hamamelis Virginiana (Witch Hazel) Extract, Butylene Glycol, Cnidium Officinale Root Extract, Lonicera Japonica (Honeysuckle) Flower Extract, Copper Tripeptide-1
- PURPOSE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- Uses
- Directions
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
CONJU PRINCESS LIFTING
adenosine creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72950-060 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Adenosine (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) Adenosine 0.02 g in 50 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Dipropylene Glycol (UNII: E107L85C40) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72950-060-02 1 in 1 CARTON 03/01/2019 1 NDC:72950-060-01 50 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 unapproved drug other 03/01/2019 Labeler - Conju Korea Inc. (694849608) Registrant - Conju Korea Inc. (694849608) Establishment Name Address ID/FEI Business Operations Conju Korea Inc. 694849608 manufacture(72950-060)