NDC 50405-002 Sohmed Acid Reducer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50405 - Sohm Inc.
- 50405-002 - Sohmed Acid Reducer
Product Characteristics
Product Packages
NDC Code 50405-002-50
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON / 50 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC
Product Details
What is NDC 50405-002?
What are the uses for Sohmed Acid Reducer?
Which are Sohmed Acid Reducer UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) (Active Moiety)
- MAGNESIUM CARBONATE (UNII: 0E53J927NA)
- CARBONATE ION (UNII: 7UJQ5OPE7D) (Active Moiety)
Which are Sohmed Acid Reducer 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 Sohmed Acid Reducer?
- RxCUI: 308072 - aluminum hydroxide 160 MG / magnesium carbonate 105 MG Chewable Tablet
* 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".