NDC 54868-2399 Calcium Carbonate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-2399 - Calcium Carbonate
Product Characteristics
YELLOW (C48330)
GREEN (C48329)
ORANGE (C48331)
Product Packages
NDC Code 54868-2399-1
Package Description: 60 TABLET, CHEWABLE in 1 BOTTLE
Product Details
What is NDC 54868-2399?
What are the uses for Calcium Carbonate?
Which are Calcium Carbonate UNII Codes?
The UNII codes for the active ingredients in this product are:
- CALCIUM CARBONATE (UNII: H0G9379FGK)
- CALCIUM CATION (UNII: 2M83C4R6ZB) (Active Moiety)
- CARBONATE ION (UNII: 7UJQ5OPE7D) (Active Moiety)
Which are Calcium Carbonate 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:
- ADIPIC ACID (UNII: 76A0JE0FKJ)
- DEXTROSE (UNII: IY9XDZ35W2)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- MINERAL OIL (UNII: T5L8T28FGP)
- POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)
- POWDERED CELLULOSE (UNII: SMD1X3XO9M)
- TALC (UNII: 7SEV7J4R1U)
What is the NDC to RxNorm Crosswalk for Calcium Carbonate?
- RxCUI: 359297 - calcium carbonate 1250 MG (Ca 500 MG) Chewable Tablet
- RxCUI: 359297 - calcium carbonate 1250 MG Chewable Tablet
- RxCUI: 359297 - calcium carbonate 1250 MG (calcium 500 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".