NDC 58133-956 Relieveit Footspray Topical Analgesic
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 58133-956?
What are the uses for Relieveit Footspray Topical Analgesic?
Which are Relieveit Footspray Topical Analgesic UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Relieveit Footspray Topical Analgesic 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:
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- CYCLOMETHICONE (UNII: NMQ347994Z)
- BIS-ETHOXYDIGLYCOL CYCLOHEXANE 1,4-DICARBOXYLATE (UNII: R6MU0U9L45)
- HARPAGOPHYTUM PROCUMBENS ROOT (UNII: 1OYM338E89)
- ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
- LEMON OIL (UNII: I9GRO824LL)
- EAST INDIAN LEMONGRASS OIL (UNII: UP0M8M3VZW)
- PEPPERMINT (UNII: V95R5KMY2B)
- TEA TREE OIL (UNII: VIF565UC2G)
- ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
- 1-(3-AMINO-4-HYDROXYPHENYL)-2-((2-(4-METHOXYPHENYL)-1-METHYLETHYL)AMINO)ETHANOL (UNII: GJY78AX70Q)
- PINUS RESINOSA WHOLE (UNII: AS8B4M6X9N)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- PROPYLENE GLYCOL 1-ALLYL ETHER (UNII: QRB8092KPK)
* 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".