Label: ALOE COAL 01- pyrithione zinc liquid
- NDC Code(s): 73324-091-08
- Packager: T. SPRUILL, LLC
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated November 11, 2023
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- Drug Facts
- ACTIVE INGREDIENT:
- USES:
- WARNINGS
- DIRECTIONS:
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OTHER INGREDIENTS:
Activated Charcoal Powder, Aloe Barbadensis (Aloe Vera Gel) Juice, Aqua (Deionized Water), Argania Spinosa (Argan) Oil, Avena Sativa (Oat) Protein, Biotin, Citrus Grandis (Grapefruit) Oil, Cocamidopropyl Betaine, Dimethicone, Equisetum Arvense (Horsetail) Extract, Ethylhexylglycerin, Glycerin, Helianthus Annuus (Sunflower) Oil, Hydrolyzed Rice Protein, Olea Europaea (Olive) Oil, Lauryl Glucoside, di-Panthenol, Phenoxyethanol, Rosa Canina (Rose Hips) Oil, Simmondsia Chinensis (Jojoba) Oil, Sodium C14-16 Alpha Olefin Sulfonate, Sodium Cocoyl Isethionate, Sodium Lauryl Glucose Carboxylate
- Package Labeling:
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INGREDIENTS AND APPEARANCE
ALOE COAL 01
pyrithione zinc liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73324-091 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5) PYRITHIONE ZINC 10 mg in 1 mL Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) WATER (UNII: 059QF0KO0R) ARGAN OIL (UNII: 4V59G5UW9X) OAT (UNII: Z6J799EAJK) BIOTIN (UNII: 6SO6U10H04) GRAPEFRUIT (UNII: O82C39RR8C) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) DIMETHICONE (UNII: 92RU3N3Y1O) EQUISETUM ARVENSE BRANCH (UNII: 1L0VKZ185E) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) GLYCERIN (UNII: PDC6A3C0OX) HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP) OLEA EUROPAEA (OLIVE) OIL UNSAPONIFIABLES (UNII: XO45V955LT) LAURYL GLUCOSIDE (UNII: 76LN7P7UCU) PHENOXYETHANOL (UNII: HIE492ZZ3T) ROSA CANINA FRUIT (UNII: 3TNW8D08V3) JOJOBA OIL (UNII: 724GKU717M) SODIUM COCOYL ISETHIONATE (UNII: 518XTE8493) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73324-091-08 237 mL in 1 BOTTLE; Type 0: Not a Combination Product 08/26/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M032 08/26/2019 Labeler - T. SPRUILL, LLC (117054436)