NDC 70236-101 C-patch Grande
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 70236 - Neobiotech Global Corporation
- 70236-101 - C-patch Grande
Product Packages
NDC Code 70236-101-02
Package Description: 6 PATCH in 1 POUCH / 28 g in 1 PATCH (70236-101-01)
Product Details
What is NDC 70236-101?
What are the uses for C-patch Grande?
Which are C-patch Grande UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (Active Moiety)
Which are C-patch Grande 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:
- TARTARIC ACID (UNII: W4888I119H)
- SORBITOL (UNII: 506T60A25R)
- ACTIVATED CHARCOAL (UNII: 2P3VWU3H10)
- GELATIN (UNII: 2G86QN327L)
- DIHYDROXYALUMINUM AMINOACETATE ANHYDROUS (UNII: 1K713C615K)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- GLYCERIN (UNII: PDC6A3C0OX)
- POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)
- WATER (UNII: 059QF0KO0R)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
What is the NDC to RxNorm Crosswalk for C-patch Grande?
- RxCUI: 1997510 - camphor 0.5 % / menthol 2.5 % Medicated Patch
- RxCUI: 1997510 - camphor 0.005 MG/MG / menthol 0.025 MG/MG Medicated Patch
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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".