NDC 24909-604 Fastrin Aches And Pain Deep Relief
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 24909 - Aidance Skincare & Topical Solutions, Llc
- 24909-604 - Fastrin Aches And Pain Deep Relief
Product Packages
NDC Code 24909-604-10
Package Description: 10 g in 1 JAR
NDC Code 24909-604-50
Package Description: 50 g in 1 TUBE
Product Details
What is NDC 24909-604?
What are the uses for Fastrin Aches And Pain Deep Relief?
Which are Fastrin Aches And Pain Deep Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (Active Moiety)
Which are Fastrin Aches And Pain Deep Relief 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:
- CLOVE OIL (UNII: 578389D6D0)
- CORYMBIA CITRIODORA LEAF OIL (UNII: M63U6N96EB)
- COTTONSEED OIL (UNII: H3E878020N)
- JOJOBA OIL (UNII: 724GKU717M)
- MAGNESIUM OXIDE (UNII: 3A3U0GI71G)
- PEPPERMINT OIL (UNII: AV092KU4JH)
- SILVER OXIDE (UNII: 897WUN6G6T)
- SORBIC ACID (UNII: X045WJ989B)
- TEA TREE OIL (UNII: VIF565UC2G)
- WHITE WAX (UNII: 7G1J5DA97F)
- ZINC OXIDE (UNII: SOI2LOH54Z)
What is the NDC to RxNorm Crosswalk for Fastrin Aches And Pain Deep Relief?
- RxCUI: 1802734 - camphor 11 % / menthol 16 % Topical Ointment
- RxCUI: 1802734 - camphor 0.11 MG/MG / menthol 0.16 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".