NDC 58443-0243 Australian Gold Metro 365 Medicated Leave-in Treatment Step 3
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 58443 - Prime Enterprises Inc.
- 58443-0243 - Australian Gold
Product Characteristics
Product Packages
NDC Code 58443-0243-3
Package Description: 118 mL in 1 TUBE
Product Details
What is NDC 58443-0243?
What are the uses for Australian Gold Metro 365 Medicated Leave-in Treatment Step 3?
Which are Australian Gold Metro 365 Medicated Leave-in Treatment Step 3 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 Australian Gold Metro 365 Medicated Leave-in Treatment Step 3 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:
- CHLORPHENESIN (UNII: I670DAL4SZ)
- CETRIMONIUM BROMIDE (UNII: L64N7M9BWR)
- PALM OIL (UNII: 5QUO05548Z)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- GLYCERIN (UNII: PDC6A3C0OX)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- WATER (UNII: 059QF0KO0R)
- GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE) (UNII: B16G315W7A)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
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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".