NDC 72029-001 Revox
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
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Product Details
What is NDC 72029-001?
What are the uses for Revox?
Which are Revox UNII Codes?
The UNII codes for the active ingredients in this product are:
- PYRITHIONE ZINC (UNII: R953O2RHZ5)
- PYRITHIONE ZINC (UNII: R953O2RHZ5) (Active Moiety)
Which are Revox 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:
- WATER (UNII: 059QF0KO0R)
- SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW) (UNII: 0L414VCS5Y)
- COCO DIETHANOLAMIDE (UNII: 92005F972D)
- BETULA PUBESCENS LEAF (UNII: 84SOH0O3OO)
- CHAMOMILE (UNII: FGL3685T2X)
- MILLET (UNII: TJR6B3R47P)
- SAGE (UNII: 065C5D077J)
- URTICA DIOICA LEAF (UNII: X6M0DRN46Q)
- EQUISETUM ARVENSE BRANCH (UNII: 1L0VKZ185E)
- HOPS (UNII: 01G73H6H83)
- CINCHONA PUBESCENS BARK (UNII: S96N10R972)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- TILIA CORDATA FLOWER (UNII: CFN6G1F6YK)
- PANTHENOL (UNII: WV9CM0O67Z)
- NIACIN (UNII: 2679MF687A)
- BIOTIN (UNII: 6SO6U10H04)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- HYDROLYZED WHEAT PROTEIN (ENZYMATIC, 3000 MW) (UNII: J2S07SB0YL)
- CANANGA OIL (UNII: 8YOY78GNNX)
- DEXPANTHENOL (UNII: 1O6C93RI7Z)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ECHINACEA PURPUREA (UNII: QI7G114Y98)
- CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
- CENTELLA ASIATICA (UNII: 7M867G6T1U)
- MELISSA OFFICINALIS LEAF (UNII: 50D2ZE9219)
- HAMAMELIS VIRGINIANA LEAF (UNII: T07U1161SV)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- VITIS VINIFERA SEED (UNII: C34U15ICXA)
- POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
- TOCOPHEROL (UNII: R0ZB2556P8)
- PEA (UNII: W4X7H8GYFM)
- EDETATE SODIUM (UNII: MP1J8420LU)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- COUMARIN (UNII: A4VZ22K1WT)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
- METHYL-.ALPHA.-IONONE (UNII: QMK5X3FBG7)
- LINALYL ACETATE (UNII: 5K47SSQ51G)
What is the NDC to RxNorm Crosswalk for Revox?
- RxCUI: 244458 - zinc pyrithione 2 % Medicated Shampoo
- RxCUI: 244458 - zinc pyrithione 20 MG/ML Medicated Shampoo
* 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".