NDC 54576-3001 Roota Re F Tonic
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 54576-3001?
What are the uses for Roota Re F Tonic?
Which are Roota Re F 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 F 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)
- GLYCOLIC ACID (UNII: 0WT12SX38S)
- GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
- CAMPHOR (NATURAL) (UNII: N20HL7Q941)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- MENTHA PIPERITA (UNII: 79M2M2UDA9)
- ALLANTOIN (UNII: 344S277G0Z)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- ZINC SULFATE (UNII: 89DS0H96TB)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- ROSEMARY (UNII: IJ67X351P9)
- NIACINAMIDE (UNII: 25X51I8RD4)
- ASIAN GINSENG (UNII: CUQ3A77YXI)
- PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV)
- SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K)
- ACORUS CALAMUS ROOT (UNII: XY1K7KIQ0F)
- FALLOPIA MULTIFLORA ROOT (UNII: AUZ3VD75MC)
- MORUS ALBA BARK (UNII: 7O71A48NDP)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
- GINKGO (UNII: 19FUJ2C58T)
- PREZATIDE COPPER (UNII: 6BJQ43T1I9)
What is the NDC to RxNorm Crosswalk for Roota Re F Tonic?
- RxCUI: 1365693 - panthenol 0.5 MG per 100 ML Topical Solution
- RxCUI: 1365693 - panthenol 0.005 MG/ML Topical Solution
* 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".