NDC 75974-100 Anc Neverpain External Analgesic
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What is NDC 75974-100?
What are the uses for Anc Neverpain External Analgesic?
Which are Anc Neverpain External Analgesic UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Anc Neverpain External 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:
- ALCOHOL (UNII: 3K9958V90M)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
- PEPPERMINT (UNII: V95R5KMY2B)
- COPAIFERA OFFICINALIS RESIN (UNII: 1VH544O5AT)
- PASSIFLORA INCARNATA FLOWER (UNII: K8F3G29S6Z)
What is the NDC to RxNorm Crosswalk for Anc Neverpain External Analgesic?
- RxCUI: 1094550 - menthol 5 % Topical Spray
- RxCUI: 1094550 - menthol 50 MG/ML Topical Spray
- RxCUI: 1872081 - NEVERPAIN 5 % Topical Spray
- RxCUI: 1872081 - menthol 50 MG/ML Topical Spray [NEVERPAIN]
- RxCUI: 1872081 - NEVERPAIN 50 MG/ML Topical Spray
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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".