NDC 76081-010 Damoae Therapy
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 76081-010?
What are the uses for Damoae Therapy?
Which are Damoae Therapy UNII Codes?
The UNII codes for the active ingredients in this product are:
- PYRITHIONE ZINC (UNII: R953O2RHZ5)
- PYRITHIONE (UNII: 6GK82EC25D) (Active Moiety)
Which are Damoae Therapy Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- BIOTIN (UNII: 6SO6U10H04)
- NIACINAMIDE (UNII: 25X51I8RD4)
- DEXPANTHENOL (UNII: 1O6C93RI7Z)
- DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- MENTHA PIPERITA LEAF (UNII: A389O33LX6)
- CITRUS RETICULATA FRUIT OIL (UNII: 25P9H3QU5E)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- FALLOPIA MULTIFLORA ROOT (UNII: AUZ3VD75MC)
- POLYQUATERNIUM-10 (400 CPS AT 2%) (UNII: HB1401PQFS)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- ROSEMARY OIL (UNII: 8LGU7VM393)
- OENOTHERA BIENNIS FLOWERING TOP (UNII: I3Z7321G2F)
- LEVOMENTHOL (UNII: BZ1R15MTK7)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Damoae Therapy?
- RxCUI: 209884 - zinc pyrithione 1 % Medicated Shampoo
- RxCUI: 209884 - zinc pyrithione 10 MG/ML Medicated Shampoo
- RxCUI: 209884 - zinc pyrithione 1 % Medicated Conditioner
* Please review the disclaimer below.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".