NDC 70859-030 Nudroxipak I-800
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
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Product Details
What is NDC 70859-030?
What are the uses for Nudroxipak I-800?
Which are Nudroxipak I-800 UNII Codes?
The UNII codes for the active ingredients in this product are:
- CAPSAICIN (UNII: S07O44R1ZM)
- CAPSAICIN (UNII: S07O44R1ZM) (Active Moiety)
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
- IBUPROFEN (UNII: WK2XYI10QM)
- IBUPROFEN (UNII: WK2XYI10QM) (Active Moiety)
Which are Nudroxipak I-800 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:
- ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- INDIAN FRANKINCENSE (UNII: 4PW41QCO2M)
- SORBITAN OLIVATE (UNII: MDL271E3GR)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
- CETEARYL OLIVATE (UNII: 58B69Q84JO)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB)
- ILEX PARAGUARIENSIS LEAF (UNII: 1Q953B4O4F)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- WATER (UNII: 059QF0KO0R)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
- CROSCARMELLOSE (UNII: 029TFK992N)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- POLYDEXTROSE (UNII: VH2XOU12IE)
- POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
What is the NDC to RxNorm Crosswalk for Nudroxipak I-800?
- RxCUI: 197807 - ibuprofen 800 MG Oral Tablet
- RxCUI: 1989491 - capsaicin 0.025 % / menthol 6 % / methyl salicylate 25 % Topical Solution
- RxCUI: 1989491 - capsaicin 0.25 MG/ML / menthol 60 MG/ML / methyl salicylate 250 MG/ML Topical Solution
- RxCUI: 206917 - Ibu 800 MG Oral Tablet
- RxCUI: 206917 - ibuprofen 800 MG Oral Tablet [Ibu]
* 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".