Label: AT ALPHA- glycerin cream
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Contains inactivated NDC Code(s)
NDC Code(s): 70141-010-01 - Packager: SALOJE Inc
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated October 6, 2015
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- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Inactive Ingredients: Water, Butylene Glycol, Caprylic/Capric Triglyceride, Betaine, Cetearyl Alcohol, Butylene Glycol Dicaprylate/Dicaprate, Squalane, Sorbitan Stearate, Stearic Acid, Polyglyceryl-10 Distearate, Glyceryl Stearate, Dimethicone, Sodium Hyaluronate, Aureobasidium Pullulans Ferment Filtrate, Tocopheryl Acetate, Portulaca Oleracea Extract, Aloe Barbadensis Leaf Juice, Rehmannia Chinensis Root Extract, Schizonepeta Tenuifolia Extract, Saururus Chinensis Leaf/Root Extract, Polygonum Fagopyrum (Buckwheat) Seed Extract, Glycine Max (Soybean) Seed Extract, Acanthopanax Senticosus (Eleuthero) Root Extract, Ulmus Davidiana Root Extract, Poria Cocos Extract, Ginkgo Biloba Leaf Extract, Prunus Armeniaca (Apricot) Kernel Extract, Sanguisorba Officinalis Root Extract, Phellodendron Amurense Bark Extract, Prunus Mume Fruit Extract, Zanthoxylum Piperitum Fruit Extract, Pinus Densiflora Extract, Magnolia Obovata Bark Extract, Polygonum Cuspidatum Root Extract, Sophora Angustifolia Root Extract, Camellia Sinensis Leaf Extract, Ganoderma Lucidum (Mushroom) Stem Extract, Carthamus Tinctorius (Safflower) Flower Extract, Oryza Sativa (Rice) Bran Extract, Bletia Hyacinthina Bulb Extract, Allantoin, 1,2-Hexanediol, Propanediol, Caprylyl Glycol, Illicium Verum (Anise) Fruit Extract, Arginine, Carbomer, Alloferon-1
- PURPOSE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
AT ALPHA
glycerin creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70141-010 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Glycerin (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) Glycerin 5 mg in 50 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Butylene Glycol (UNII: 3XUS85K0RA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70141-010-01 50 mL in 1 CARTON; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 09/01/2015 Labeler - SALOJE Inc (689516928) Registrant - SALOJE Inc (689516928) Establishment Name Address ID/FEI Business Operations SALOJE Inc 689516928 manufacture(70141-010)