NDC 70859-033 Nudroxipak Dsdr-50
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 70859 - Nucare Pharmaceuticals, Inc.
- 70859-033 - Nudroxipak Dsdr-50
Product Characteristics
Product Packages
NDC Code 70859-033-01
Package Description: 1 KIT in 1 CARTON * 1 CONTAINER in 1 CARTON (70859-028-03) / 90 mL in 1 CONTAINER * 60 TABLET, DELAYED RELEASE in 1 BOTTLE (0228-2550-06)
Product Details
What is NDC 70859-033?
What are the uses for Nudroxipak Dsdr-50?
Which are Nudroxipak Dsdr-50 UNII Codes?
The UNII codes for the active ingredients in this product are:
- DICLOFENAC SODIUM (UNII: QTG126297Q)
- DICLOFENAC (UNII: 144O8QL0L1) (Active Moiety)
- CAPSAICIN (UNII: S07O44R1ZM)
- CAPSAICIN (UNII: S07O44R1ZM) (Active Moiety)
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Nudroxipak Dsdr-50 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:
- POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
- ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- SODIUM ALGINATE (UNII: C269C4G2ZQ)
- TALC (UNII: 7SEV7J4R1U)
- POLYVINYL ACETATE PHTHALATE (UNII: 58QVG85GW3)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- SORBITAN OLIVATE (UNII: MDL271E3GR)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- ILEX PARAGUARIENSIS LEAF (UNII: 1Q953B4O4F)
- MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB)
- WATER (UNII: 059QF0KO0R)
- ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
- INDIAN FRANKINCENSE (UNII: 4PW41QCO2M)
- CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
- CETEARYL OLIVATE (UNII: 58B69Q84JO)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- YELLOW WAX (UNII: 2ZA36H0S2V)
What is the NDC to RxNorm Crosswalk for Nudroxipak Dsdr-50?
- 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: 855906 - diclofenac sodium 50 MG Delayed Release Oral Tablet
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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".