NDC 71105-303 Mint Flavored Antacid
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 71105 - Redicare Llc
- 71105-303 - Mint Flavored Antacid
Product Characteristics
Product Packages
NDC Code 71105-303-68
Package Description: 100 TABLET, CHEWABLE in 1 CARTON
Product Details
What is NDC 71105-303?
What are the uses for Mint Flavored Antacid?
Which are Mint Flavored Antacid 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 Mint Flavored Antacid 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)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- SUCROSE (UNII: C151H8M554)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- MINT (UNII: FV98Z8GITP)
What is the NDC to RxNorm Crosswalk for Mint Flavored Antacid?
- 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
* Please review the disclaimer below.
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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* 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".