Label: LECINQ PREBENONE SERUM- niacinamide, adenosine liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 73114-010-01, 73114-010-02 - Packager: Lecinq Co., Ltd.
- 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 May 17, 2019
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Inactive ingredients:
Water,Butylene Glycol,Panthenol,Glyceryl Glucoside,Propanediol,Glycerin,1,2-Hexanediol,Hydroxydecyl Ubiquinone,Sodium Ascorbyl Phosphate,Alteromonas Ferment Extract,Sodium Hyaluronate,Hydrolyzed Hyaluronic Acid,Sodium Acetylated Hyaluronate,Yeast Extract,Pancratium Maritimum Extract,Glutathione,Citrus Paradisi (Grapefruit) Fruit Extract,Fructan,Citrus Tangerina (Tangerine) Peel Oil,Pelargonium Graveolens Flower Oil,Lavandula Angustifolia (Lavender) Oil,Argania Spinosa Kernel Oil,Soluble Collagen,Squalane,Glucose,Hydroxyethylcellulose,Chondrus Crispus Powder,Agar,Buteth-3,Sodium Benzotriazolyl Butylphenol Sulfonate,Acrylates/C10-30 Alkyl Acrylate Crosspolymer,Hydrogenated Lecithin,Tributyl Citrate,Gellan Gum,Carbomer,Tromethamine,C12-13 Pareth-9,Ethylhexylglycerin,Disodium EDTA,Chlorphenesin,CI 77491,CI 77492
- PURPOSE
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WARNINGS
Warnings:
For external use only
- Do not use on damaged or broken skin
- When using this product, Keep out of eyes. Rinse with water to remove.
- Stop use and ask a doctor if rash occurs.
- Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away. - KEEP OUT OF REACH OF CHILDREN
- Uses
- Directions
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
LECINQ PREBENONE SERUM
niacinamide, adenosine liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73114-010 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Niacinamide (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) Niacinamide 0.70 g in 35 mL Adenosine (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) Adenosine 0.01 g in 35 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Butylene Glycol (UNII: 3XUS85K0RA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73114-010-02 1 in 1 CARTON 04/01/2019 1 NDC:73114-010-01 35 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 04/01/2019 Labeler - Lecinq Co., Ltd. (695716823) Registrant - Lecinq Co., Ltd. (695716823) Establishment Name Address ID/FEI Business Operations CELLAB CO., LTD. 688195494 manufacture(73114-010)
