NDC 71419-001 Magic For Pain Relief
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 71419-001?
What are the uses for Magic For Pain Relief?
Which are Magic For Pain Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (Active Moiety)
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Magic For Pain 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:
- CARTHAMUS TINCTORIUS WHOLE (UNII: 5EMV416J82)
- CAPSICUM ANNUUM WHOLE (UNII: 7FKZ3QQQ1F)
- PANAX NOTOGINSENG ROOT (UNII: GQX1C1175U)
- REHMANNIA GLUTINOSA ROOT (UNII: 1BEM3U6LQQ)
- ANGELICA PUBESCENS ROOT (UNII: 0MF1EI01KJ)
- DAEMONOROPS DRACO WHOLE (UNII: 1C8HA8O22C)
- VANILLYL BUTYL ETHER (UNII: S2ULN37C9R)
- MUSCONE (UNII: UPS3C6CV36)
- BORNEOL (UNII: M89NIB437X)
- ALCOHOL (UNII: 3K9958V90M)
What is the NDC to RxNorm Crosswalk for Magic For Pain Relief?
- RxCUI: 1941591 - menthol 16 % / methyl salicylate 30 % / synthetic camphor 10 % Topical Spray
- RxCUI: 1941591 - menthol 160 MG/ML / methyl salicylate 300 MG/ML / synthetic camphor 100 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".