NDC 24909-132 Terrasil Skin Repair Max
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 24909 - Aidance Skincare & Topical Solutions, Llc
- 24909-132 - Terrasil Skin Repair
Product Packages
NDC Code 24909-132-14
Package Description: 14 g in 1 JAR
NDC Code 24909-132-44
Package Description: 44 g in 1 JAR
Product Details
What is NDC 24909-132?
What are the uses for Terrasil Skin Repair Max?
Which are Terrasil Skin Repair Max UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALLANTOIN (UNII: 344S277G0Z)
- ALLANTOIN (UNII: 344S277G0Z) (Active Moiety)
- BENZETHONIUM CHLORIDE (UNII: PH41D05744)
- BENZETHONIUM (UNII: 1VU15B70BP) (Active Moiety)
Which are Terrasil Skin Repair Max 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:
- BENTONITE (UNII: A3N5ZCN45C)
- CEDRUS DEODARA WOOD OIL (UNII: 01O086PVD0)
- JOJOBA OIL (UNII: 724GKU717M)
- MAGNESIUM OXIDE (UNII: 3A3U0GI71G)
- PEPPERMINT OIL (UNII: AV092KU4JH)
- SILVER OXIDE (UNII: 897WUN6G6T)
- TEA TREE OIL (UNII: VIF565UC2G)
- WHITE WAX (UNII: 7G1J5DA97F)
- ZINC OXIDE (UNII: SOI2LOH54Z)
What is the NDC to RxNorm Crosswalk for Terrasil Skin Repair Max?
- RxCUI: 1250637 - allantoin 1 % / benzethonium chloride 0.2 % Topical Ointment
- RxCUI: 1250637 - allantoin 0.01 MG/MG / benzethonium chloride 0.002 MG/MG Topical Ointment
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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".