Label: APPLICELL PERFECT EYE- adenosine cream
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Contains inactivated NDC Code(s)
NDC Code(s): 71098-050-01, 71098-050-02 - Packager: Anc HnB Inc.
- 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 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, Dipropylene Glycol, Hydrogenated Polydecene, Cyclopentasiloxane, Cyclohexasiloxane, Hydrolyzed Keratin, Hydrolyzed Collagen, Hydrolyzed Elastin, Cetearyl Alcohol, Polyglyceryl-3 Methylglucose Distearate, Betaine, Butyrospermum Parkii(Shea Butter), Neopentyl Glycol Dicaprate, Dimethicone, Triethylhexanoin, Glyceryl Stearate SE, Sodium Hyaluronate, Human fibroblast Conditioned Media, Stearic Acid, Beeswax, PEG-100 Stearate, Citrus Paradisi (Grapefruit) Fruit Extract, Glyceryl Stearate, Tocopheryl Acetate, Xanthan Gum, Ceramide 3, Hydrogenated Lecithin, Neofinetia Falcata Callus Culture Extract, Caprylhydroxamic Acid, Caprylyl Glycol, Phenoxyethanol, Carbomer, Potassium Hydroxide, 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 PERFECT EYE
adenosine creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71098-050 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 30 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:71098-050-02 1 in 1 CARTON 10/10/2016 1 NDC:71098-050-01 30 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(71098-050)
