Label: APPLICELL INTENSIVE SERUM- adenosine cream
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Contains inactivated NDC Code(s)
NDC Code(s): 71098-030-01, 71098-030-02 - Packager: Anc HnB Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated November 25, 2016
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, Glycerin, Portulaca Oleracea Extract, Hydrolyzed Keratin, Hydrolyzed Collagen, Hydrolyzed Elastin, Dipropylene Glycol, Hydrogenated Polydecene, Cyclopentasiloxane, Cyclohexasiloxane, Neopentyl Glycol Dicaprate, Caprylic/Capric Triglyceride, Cetearyl Alcohol, Citrus Paradisi (Grapefruit) Fruit Extract, Hydrogenated Lecithin, Glyceryl Stearate SE, Human fibroblast Conditioned Media, Carbomer, Neofinetia Falcata Callus Culture Extract, Beeswax, Macadamia Ternifolia Seed Oil, Betaine, Trehalose, Coix Lacryma-Jobi Ma-yuen Seed Extract, Tocopheryl Acetate, Potassium Hydroxide, Dimethicone, Xanthan Gum, Caprylhydroxamic Acid, Caprylyl Glycol, Phenoxyethanol, Trisodium EDTA, Fragrance
- PURPOSE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
APPLICELL INTENSIVE SERUM
adenosine creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71098-030 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Adenosine (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) Adenosine 0.01 g in 45 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Glycerin (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71098-030-02 1 in 1 CARTON 10/10/2016 1 NDC:71098-030-01 45 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 10/10/2016 Labeler - Anc HnB Inc. (689031836) Registrant - Anc HnB Inc. (689031836) Establishment Name Address ID/FEI Business Operations Anc HnB Inc. 689031836 manufacture(71098-030)
