Label: APPLICELL MIRACLE- adenosine cream
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Contains inactivated NDC Code(s)
NDC Code(s): 71098-040-01, 71098-040-02 - 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, Cyclopentasiloxane, Cyclohexasiloxane, Portulaca Oleracea Extract, Hydrolyzed Keratin, Hydrolyzed Collagen, Hydrolyzed Elastin, Dipropylene Glycol, Glycerin, Butylene Glycol, Neopentyl Glycol Dicaprate, Caprylic/Capric Triglyceride, Betaine, Cetyl Ethylhexanoate, Cetearyl Alcohol, Butyrospermum Parkii(Shea Butter), Sodium Hyaluronate, Glyceryl Stearate SE, PEG-40 Stearate, Sorbitan Stearate, Stearic Acid, Citrus Paradisi (Grapefruit) Fruit Extract, Neofinetia Falcata Callus Culture Extract, Beeswax, Xanthan Gum, Carbomer, Trehalose, Human fibroblast Conditioned Media, Dipotassium Glycyrrhizate , Caprylhydroxamic Acid, Caprylyl Glycol, Coix Lacryma-Jobi Ma-yuen Seed Extract, Phenoxyethanol, Potassium Hydroxide, Hydrogenated Lecithin, Ceramide 3, Macadamia Ternifolia Seed Oil, Trehalose, 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 MIRACLE
adenosine creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71098-040 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:71098-040-02 1 in 1 CARTON 10/10/2016 1 NDC:71098-040-01 50 mL in 1 BOTTLE, PLASTIC; 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(71098-040)
