Label: DERMAHARMONY SEBORRHEIC DERMATITIS- pyrithione zinc cream
- NDC Code(s): 71819-002-03, 71819-002-06, 71819-002-08
- Packager: D3 Development, Inc.
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated October 26, 2020
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- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- ASK DOCTOR
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- STORAGE AND HANDLING
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INACTIVE INGREDIENT
Inactive ingredients
Water, prunus amygdalus dulcis (sweet almond) oil, persea gratissima (avocado) oil, behentrimonium methosulfate, cetyl alcohol, glycerin, coco nucifera (coconut) oil, ricinus communis (castor) oil, stearyl alcohol, beeswax, shea butter, mango seed butter, phenoxyethanol, caprylyl glycol, tocopherol (vitamin E), hydroxyethylcellulose
- QUESTIONS
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
DERMAHARMONY SEBORRHEIC DERMATITIS
pyrithione zinc creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71819-002 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5) PYRITHIONE ZINC 0.25 g in 100 mL Inactive Ingredients Ingredient Name Strength PHENOXYETHANOL (UNII: HIE492ZZ3T) YELLOW WAX (UNII: 2ZA36H0S2V) GLYCERIN (UNII: PDC6A3C0OX) CAPRYLYL GLYCOL (UNII: 00YIU5438U) TOCOPHEROL (UNII: R0ZB2556P8) HYDROXYETHYL CELLULOSE (1800 MPA.S AT 2%) (UNII: 6OX6A5C7B6) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) ALMOND OIL (UNII: 66YXD4DKO9) WATER (UNII: 059QF0KO0R) AVOCADO OIL (UNII: 6VNO72PFC1) CETYL ALCOHOL (UNII: 936JST6JCN) COCONUT OIL (UNII: Q9L0O73W7L) CASTOR OIL (UNII: D5340Y2I9G) BEHENTRIMONIUM METHOSULFATE (UNII: 5SHP745C61) SHEA BUTTER (UNII: K49155WL9Y) MANGIFERA INDICA SEED BUTTER (UNII: 4OXD9M35X2) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71819-002-03 89 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/26/2019 2 NDC:71819-002-06 177 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/26/2020 3 NDC:71819-002-08 237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/26/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part358H 07/26/2019 Labeler - D3 Development, Inc. (043195877)