NDC 81238-0303 Aramark Antacid Chewable
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 81238-0303?
What are the uses for Aramark Antacid Chewable?
Which are Aramark Antacid Chewable UNII Codes?
The UNII codes for the active ingredients in this product are:
- CALCIUM CARBONATE (UNII: H0G9379FGK)
- CALCIUM CATION (UNII: 2M83C4R6ZB) (Active Moiety)
Which are Aramark Antacid Chewable 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:
- STARCH, CORN (UNII: O8232NY3SJ)
- SUCROSE (UNII: C151H8M554)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- MINT (UNII: FV98Z8GITP)
- ACACIA (UNII: 5C5403N26O)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
What is the NDC to RxNorm Crosswalk for Aramark Antacid Chewable?
- RxCUI: 313884 - calcium carbonate 420 MG (Ca 168 MG) Chewable Tablet
- RxCUI: 313884 - calcium carbonate 420 MG Chewable Tablet
- RxCUI: 313884 - calcium carbonate 420 MG (calcium 168 MG) Chewable Tablet
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Patient Education
Calcium Carbonate
Calcium carbonate is a dietary supplement used when the amount of calcium taken in the diet is not enough. Calcium is needed by the body for healthy bones, muscles, nervous system, and heart. Calcium carbonate also is used as an antacid to relieve heartburn, acid indigestion, and upset stomach. It is available with or without a prescription. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.
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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".