Label: TIME RETURN MELATONIN- niacinamide, adenosine patch
-
Contains inactivated NDC Code(s)
NDC Code(s): 69058-610-01, 69058-610-02, 69058-610-03, 69058-610-04 - Packager: N&B LAB.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 November 1, 2018
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
-
INACTIVE INGREDIENT
Inactive ingredients:
*Apium Graveolens (Celery) Extract, *Prunus Avium (Sweet Cherry) Fruit Extract, *Glycerin, Butylene Glycol, Propanediol, Octyldodecanol, *Caprylic/Capric Triglyceride, Cetyl Ethylhexanoate, Hydrogenated Polydecene, Methyl Hydrogenated Rosinate, Boron Nitride, Cetearyl Alcohol, Cyclopentasiloxane, 1,2-Hexanediol, Polysorbate 60, Glyceryl Stearate, PEG/PPG-17/6 Copolymer, *Olea Europaea (Olive) Fruit Oil, *Melatonin(2,500 ppm), Hydrogenated Lecithin, Polyquaternium-51, Ceramide NP, Lavandula Angustifolia (Lavender) Extract, Oenothera Biennis (Evening Primrose) Flower Extract, Chamomilla Recutita (Matricaria) Extract, Passiflora Incarnata Extract, Lycium Chinense Fruit Extract, Glutathione, Crithmum Maritimum Callus Culture Filtrate, Hydrolyzed Hyaluronic Acid, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Dimethicone, PEG-100 Stearate, Sorbitan Stearate, Cyclohexasiloxane, Dimethiconol, Squalane, Carbomer, Tromethamine, Coptis Japonica Root Extract, Helianthus Annuus (Sunflower) Seed Oil, Anthemis Nobilis Flower Oil, Disodium EDTA, Ethylhexylglycerin, Fragrance
- PURPOSE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- Uses
- Directions
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL - product image 50g
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL - product image 25g
-
INGREDIENTS AND APPEARANCE
TIME RETURN MELATONIN
niacinamide, adenosine patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69058-610 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Niacinamide (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) Niacinamide 2.0 g in 100 g Adenosine (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) Adenosine 0.04 g in 100 g Inactive Ingredients Ingredient Name Strength Glycerin (UNII: PDC6A3C0OX) Butylene Glycol (UNII: 3XUS85K0RA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69058-610-02 1 in 1 CARTON 10/01/2018 1 NDC:69058-610-01 50 g in 1 CONTAINER; Type 0: Not a Combination Product 2 NDC:69058-610-04 1 in 1 CARTON 10/01/2018 2 NDC:69058-610-03 25 g 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 10/01/2018 Labeler - N&B LAB.Co.Ltd (690332858) Registrant - N&B LAB.Co.Ltd (690332858) Establishment Name Address ID/FEI Business Operations Cosmecca Korea Co., Ltd. 688830827 manufacture(69058-610)
