Label: DERMELEVE- aluminum acetate cream
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NDC Code(s):
81507-002-01,
81507-002-02,
81507-002-03,
81507-002-04, view more81507-002-05
- Packager: Advanced Derm Solutions LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 13, 2023
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- Active Ingredient
- Purpose
- Uses
- Warnings
- KEEP OUT OF REACH OF CHILDREN
- Directions
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Inactive ingredients
Water, Strontium Nitrate, Isopropyl Myristate, Butyrospermum Parkii (shea) Butter, Caprylyc/Capric Triglyceride, Cetearyl Alcohol, Emulsifying Wax NF, Glycerin, Phenoxyethanol, Magnesium Aluminum Silicate, Glyceryl Stearate, Dimethicone, Polyacrylate Crosspolymer-6, Xanthan Gum, Caprylyl Glycol, Sodium Hyaluronate, Disodium EDTA, Ceramide NG, Tocopherol (Vitamin E), Tetrahexyldecyl Ascorbate
- SPL UNCLASSIFIED SECTION
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- Product label
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INGREDIENTS AND APPEARANCE
DERMELEVE
aluminum acetate creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:81507-002 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALUMINUM ACETATE (UNII: 80EHD8I43D) (ALUMINUM CATION - UNII:3XHB1D032B) ALUMINUM ACETATE 0.2 g in 100 g Inactive Ingredients Ingredient Name Strength CERAMIDE NG (UNII: C04977SRJ5) GLYCERYL MONO AND DICAPRYLOCAPRATE (UNII: U72Q2I8C85) CETYL ALCOHOL (UNII: 936JST6JCN) POLYACRYLIC ACID (450000 MW) (UNII: KD3S7H73D3) HYALURONIC ACID (UNII: S270N0TRQY) CAPRYLYL GLYCOL (UNII: 00YIU5438U) DIMETHICONE 100 (UNII: RO266O364U) EDETATE DISODIUM (UNII: 7FLD91C86K) GLYCERIN (UNII: PDC6A3C0OX) GLYCERYL STEARATE SE (UNII: FCZ5MH785I) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) MAGNESIUM ALUMINUM SILICATE TYPE IA (UNII: SUS08ZOA9S) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) PHENOXYETHANOL (UNII: HIE492ZZ3T) POLAWAX POLYSORBATE (UNII: Q504PL8E0V) SHEA BUTTER (UNII: K49155WL9Y) STRONTIUM NITRATE (UNII: BDG873AQZL) TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ) TOCOPHEROL (UNII: R0ZB2556P8) WATER O-18 (UNII: 7QV8F8BYNJ) XANTHAN GUM (UNII: TTV12P4NEE) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:81507-002-01 30 g in 1 TUBE; Type 0: Not a Combination Product 06/05/2021 2 NDC:81507-002-02 60 g in 1 TUBE; Type 0: Not a Combination Product 06/05/2021 3 NDC:81507-002-03 3 g in 1 POUCH; Type 0: Not a Combination Product 06/05/2021 08/04/2022 4 NDC:81507-002-04 80 g in 1 TUBE; Type 0: Not a Combination Product 06/05/2021 5 NDC:81507-002-05 2 g in 1 POUCH; Type 0: Not a Combination Product 08/04/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M016 06/05/2021 Labeler - Advanced Derm Solutions LLC (117840544)