NDC 53041-152 Alumox
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 53041-152?
What are the uses for Alumox?
Which are Alumox 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)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE (UNII: 92RU3N3Y1O) (Active Moiety)
Which are Alumox 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:
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- STARCH, CORN (UNII: O8232NY3SJ)
- D&C RED NO. 30 (UNII: 2S42T2808B)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- DEXTROSE (UNII: IY9XDZ35W2)
- GLYCERIN (UNII: PDC6A3C0OX)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- MANNITOL (UNII: 3OWL53L36A)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- SORBITOL (UNII: 506T60A25R)
- RAW SUGAR (UNII: 8M707QY5GH)
What is the NDC to RxNorm Crosswalk for Alumox?
- RxCUI: 307747 - aluminum hydroxide 200 MG / magnesium hydroxide 200 MG / simethicone 25 MG Chewable Tablet
- RxCUI: 307747 - aluminum hydroxide 200 MG / milk of magnesia 200 MG / simethicone 25 MG Chewable Tab
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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".