Label: ELF PERM- panthenol cream
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Contains inactivated NDC Code(s)
NDC Code(s): 70072-003-01, 70072-003-02 - Packager: giod Co.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated September 5, 2015
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
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INACTIVE INGREDIENT
Propylene Glycol, Cysteamine HCl, Ethanolamine Thioglycolate, Ethanolamine, Hydrolyzed Collagen, Cetrimonium Chloride, Glycine, Sodium Carbonate, Algin, Cellulose Gum, Glutamine, Disodium EDTA, Glycerin, Alcohol, Scutellaria Baicalensis Root Extract, Camellia Sinensis Leaf Extract, Glycyrrhiza Glabra (Licorice) Root Extract, Water
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ELF PERM
panthenol creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70072-003 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PANTHENOL (UNII: WV9CM0O67Z) (PANTHENOL - UNII:WV9CM0O67Z) PANTHENOL 0.47 g in 479.39 g Inactive Ingredients Ingredient Name Strength PROPYLENE GLYCOL (UNII: 6DC9Q167V3) CYSTEAMINE HYDROCHLORIDE (UNII: IF1B771SVB) MONOETHANOLAMINE THIOGLYCOLATE (UNII: 263SH5220T) MONOETHANOLAMINE (UNII: 5KV86114PT) CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP) GLYCINE (UNII: TE7660XO1C) SODIUM CARBONATE (UNII: 45P3261C7T) SODIUM ALGINATE (UNII: C269C4G2ZQ) CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311) GLUTAMINE (UNII: 0RH81L854J) EDETATE DISODIUM (UNII: 7FLD91C86K) GLYCERIN (UNII: PDC6A3C0OX) ALCOHOL (UNII: 3K9958V90M) SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S) GREEN TEA LEAF (UNII: W2ZU1RY8B0) GLYCYRRHIZA GLABRA (UNII: 2788Z9758H) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70072-003-02 1 in 1 CARTON 09/05/2015 1 NDC:70072-003-01 479.39 g in 1 CONTAINER; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 09/05/2015 Labeler - giod Co. (689514993) Registrant - giod Co. (689514993) Establishment Name Address ID/FEI Business Operations giod Co. 689514993 manufacture(70072-003)