NDC 54576-4001 Roota Re V Tonic
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54576 - Raphabio Inc
- 54576-4001 - Roota Re V Tonic
Product Packages
NDC Code 54576-4001-1
Package Description: 100 mL in 1 BOTTLE, WITH APPLICATOR
Product Details
What is NDC 54576-4001?
What are the uses for Roota Re V Tonic?
Which are Roota Re V Tonic 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 Tonic 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)
- ALCOHOL (UNII: 3K9958V90M)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- UREA (UNII: 8W8T17847W)
- MENTHOL (UNII: L7T10EIP3A)
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- ROSA CENTIFOLIA FLOWER (UNII: CS4TE8FF7O)
- GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- SOY PROTEIN (UNII: R44IWB3RN5)
- ALLANTOIN (UNII: 344S277G0Z)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- ROSA CANINA FRUIT OIL (UNII: CR7307M3QZ)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- FICUS CARICA WHOLE (UNII: MAW09HMQ3X)
- NIACINAMIDE (UNII: 25X51I8RD4)
- PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV)
- SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K)
- ACORUS CALAMUS ROOT (UNII: XY1K7KIQ0F)
- GINKGO (UNII: 19FUJ2C58T)
- MORUS ALBA BARK (UNII: 7O71A48NDP)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
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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".