NDC 71423-001 Neuropathy Support Foot Pain Cream
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 71423-001?
What are the uses for Neuropathy Support Foot Pain Cream?
Which are Neuropathy Support Foot Pain Cream UNII Codes?
The UNII codes for the active ingredients in this product are:
- APIS MELLIFERA (UNII: 7S82P3R43Z)
- APIS MELLIFERA (UNII: 7S82P3R43Z) (Active Moiety)
- GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q)
- GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (Active Moiety)
- PSEUDOGNAPHALIUM OBTUSIFOLIUM (UNII: 36XQ854NWW)
- PSEUDOGNAPHALIUM OBTUSIFOLIUM (UNII: 36XQ854NWW) (Active Moiety)
Which are Neuropathy Support Foot Pain Cream 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:
- MENTHOL (UNII: L7T10EIP3A)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- TROLAMINE (UNII: 9O3K93S3TK)
- CAMPHOR (NATURAL) (UNII: N20HL7Q941)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- CARBOMER 940 (UNII: 4Q93RCW27E)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- STEARETH-10 (UNII: FD0913P475)
- EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6)
- GLYCERYL STEARATE CITRATE (UNII: WH8T92A065)
- STEARETH-21 (UNII: 53J3F32P58)
- CITRUS BERGAMIA LEAF OIL (UNII: ZVY8741I1V)
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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".