NDC 68737-237 Conrx Ar
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 68737-237?
What are the uses for Conrx Ar?
Which are Conrx Ar UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) (Active Moiety)
- MAGNESIUM HYDROXIDE (UNII: NBZ3QY004S)
- MAGNESIUM CATION (UNII: T6V3LHY838) (Active Moiety)
- HYDROXIDE ION (UNII: 9159UV381P) (Active Moiety)
Which are Conrx Ar 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:
- ALGINIC ACID (UNII: 8C3Z4148WZ)
- CALCIUM STEARATE (UNII: 776XM7047L)
- MANNITOL (UNII: 3OWL53L36A)
- SODIUM BICARBONATE (UNII: 8MDF5V39QO)
- STARCH, CORN (UNII: O8232NY3SJ)
- WATER (UNII: 059QF0KO0R)
- SUCROSE (UNII: C151H8M554)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- LACTOSE (UNII: J2B2A4N98G)
- DEXTROSE (UNII: IY9XDZ35W2)
- TALC (UNII: 7SEV7J4R1U)
- SUCRALOSE (UNII: 96K6UQ3ZD4)
What is the NDC to RxNorm Crosswalk for Conrx Ar?
- RxCUI: 1376207 - aluminum hydroxide 160 MG / magnesium hydroxide 105 MG Chewable 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".