NDC 54576-2001 Roota Re V For Women
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 54576-2001?
What are the uses for Roota Re V For Women?
Which are Roota Re V For Women UNII Codes?
The UNII codes for the active ingredients in this product are:
- PANTHENOL (UNII: WV9CM0O67Z)
- PANTHENOL (UNII: WV9CM0O67Z) (Active Moiety)
Which are Roota Re V For Women 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)
- COCO DIETHANOLAMIDE (UNII: 92005F972D)
- SODIUM LAUROYL SARCOSINATE (UNII: 632GS99618)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- GLYCERIN (UNII: PDC6A3C0OX)
- EDETATE SODIUM (UNII: MP1J8420LU)
- PYRITHIONE ZINC (UNII: R953O2RHZ5)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
- GLYCERYL DISTEARATE (UNII: 73071MW2KM)
- MENTHOL (UNII: L7T10EIP3A)
- ROSA CENTIFOLIA FLOWER OIL (UNII: H32V31VMWY)
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- ALLANTOIN (UNII: 344S277G0Z)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- FALLOPIA MULTIFLORA ROOT (UNII: AUZ3VD75MC)
- ROSA CANINA FRUIT OIL (UNII: CR7307M3QZ)
- SOY PROTEIN (UNII: R44IWB3RN5)
- ACORUS CALAMUS ROOT (UNII: XY1K7KIQ0F)
- FIG (UNII: TGD87RII2U)
- MORUS ALBA BARK (UNII: 7O71A48NDP)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
- GINKGO (UNII: 19FUJ2C58T)
- UREA (UNII: 8W8T17847W)
- NIACINAMIDE (UNII: 25X51I8RD4)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- CLOVE (UNII: K48IKT5321)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
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[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".