NDC 49348-632 Sunmark Smooth Antacid
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 49348 - Mckesson
- 49348-632 - Sunmark Smooth Antacid
Product Characteristics
YELLOW (C48330)
ORANGE (C48331)
PINK (C48328)
Product Packages
NDC Code 49348-632-13
Package Description: 90 TABLET, CHEWABLE in 1 BOTTLE
Product Details
What is NDC 49348-632?
What are the uses for Sunmark Smooth Antacid?
Which are Sunmark Smooth Antacid 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 Sunmark Smooth 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:
- ADIPIC ACID (UNII: 76A0JE0FKJ)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- D&C RED NO. 30 (UNII: 2S42T2808B)
- DEXTROSE (UNII: IY9XDZ35W2)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- STARCH, CORN (UNII: O8232NY3SJ)
- SORBITOL (UNII: 506T60A25R)
- SUCROSE (UNII: C151H8M554)
- TALC (UNII: 7SEV7J4R1U)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
What is the NDC to RxNorm Crosswalk for Sunmark Smooth Antacid?
- RxCUI: 308915 - calcium carbonate 750 MG (Ca 300 MG) Chewable Tablet
- RxCUI: 308915 - calcium carbonate 750 MG Chewable Tablet
- RxCUI: 308915 - calcium carbonate 750 MG (calcium 300 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".