Label: MIRACLE MOISTURIZER ESSENCE- niacinamide lotion
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Contains inactivated NDC Code(s)
NDC Code(s): 72557-002-01 - Packager: TOAS Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated September 20, 2018
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- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
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INACTIVE INGREDIENT
Water, Glycerin, Butylene Glycol, Caprylic/Capric Triglyceride, Propylene Glycol, Macadamia Integrifolia Seed Oil, Olea Europaea (Olive) Fruit Oil, Vitis Vinifera (Grape) Seed Oil, 1,2-Hexanediol, Cetearyl Alcohol, Polysorbate 60, Cyclopentasiloxane, Butyrospermum Parkii (Shea) Butter, Sorbitan Sesquioleate, Glyceryl Stearate, PEG-100 Stearate, Stearic Acid, Carbomer, Arginine, Beeswax, Fragrance, Adenosine, Sodium Hyaluronate, Citric Acid, Hydroxyethylcellulose, Centella Asiatica Extract, Tocopheryl Acetate, Polygonum Cuspidatum Root Extract, Scutellaria Baicalensis Root Extract, Ethylhexylglycerin, Camellia Sinensis Leaf Extract, Glycyrrhiza Glabra (Licorice) Root Extract, Chamomilla Recutita (Matricaria) Flower Extract, Rosmarinus Officinalis (Rosemary) Leaf Extract, Lecithin, Hydrogenated Lecithin, Oligopeptide-1
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
MIRACLE MOISTURIZER ESSENCE
niacinamide lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72557-002 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE 0.075 g in 150 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) OLIVE OIL (UNII: 6UYK2W1W1E) GRAPE SEED OIL (UNII: 930MLC8XGG) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) POLYSORBATE 60 (UNII: CAL22UVI4M) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72557-002-01 150 g in 1 CONTAINER; Type 0: Not a Combination Product 09/20/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 09/20/2018 Labeler - TOAS Co., Ltd. (694485346) Registrant - TOAS Co., Ltd. (694485346) Establishment Name Address ID/FEI Business Operations TOAS Co., Ltd. 694485346 manufacture(72557-002)