NDC 71186-002 Vilamit Mb
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Product Details
What is NDC 71186-002?
What are the uses for Vilamit Mb?
Which are Vilamit Mb UNII Codes?
The UNII codes for the active ingredients in this product are:
- METHENAMINE (UNII: J50OIX95QV)
- METHENAMINE (UNII: J50OIX95QV) (Active Moiety)
- PHENYL SALICYLATE (UNII: 28A37T47QO)
- PHENYL SALICYLATE (UNII: 28A37T47QO) (Active Moiety)
- SODIUM PHOSPHATE, MONOBASIC, ANHYDROUS (UNII: KH7I04HPUU)
- PHOSPHATE ION (UNII: NK08V8K8HR) (Active Moiety)
- METHYLENE BLUE ANHYDROUS (UNII: 8NAP7826UB)
- METHYLENE BLUE CATION (UNII: ZMZ79891ZH) (Active Moiety)
- HYOSCYAMINE SULFATE (UNII: F2R8V82B84)
- HYOSCYAMINE (UNII: PX44XO846X) (Active Moiety)
Which are Vilamit Mb 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:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- FD&C RED NO. 3 (UNII: PN2ZH5LOQY)
- AMARANTH (UNII: 37RBV3X49K)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Vilamit Mb?
- RxCUI: 1087365 - methenamine 118 MG / sodium phosphate, monobasic 40.8 MG / phenyl salicylate 36 MG / methylene blue 10 MG / hyoscyamine sulfate 0.12 MG Oral Capsule
- RxCUI: 1087365 - hyoscyamine sulfate 0.12 MG / methenamine 118 MG / methylene blue 10 MG / phenyl salicylate 36 MG / sodium phosphate, monobasic 40.8 MG Oral Capsule
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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".