NDC 41250-373 Meijer Ultra Strength Antacid Assorted Fruit
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
GREEN (C48329)
YELLOW (C48330)
ORANGE (C48331)
Code Structure Chart
Product Details
What is NDC 41250-373?
What are the uses for Meijer Ultra Strength Antacid Assorted Fruit?
Which are Meijer Ultra Strength Antacid Assorted Fruit UNII Codes?
The UNII codes for the active ingredients in this product are:
- CALCIUM CARBONATE (UNII: H0G9379FGK)
- CARBONATE ION (UNII: 7UJQ5OPE7D) (Active Moiety)
- CALCIUM CATION (UNII: 2M83C4R6ZB) (Active Moiety)
Which are Meijer Ultra Strength Antacid Assorted Fruit 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 RED NO. 27 (UNII: 2LRS185U6K)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- STARCH, CORN (UNII: O8232NY3SJ)
- SUCRALOSE (UNII: 96K6UQ3ZD4)
What is the NDC to RxNorm Crosswalk for Meijer Ultra Strength Antacid Assorted Fruit?
- RxCUI: 308892 - calcium carbonate 1000 MG (Ca 400 MG) Chewable Tablet
- RxCUI: 308892 - calcium carbonate 1000 MG Chewable Tablet
- RxCUI: 308892 - calcium carbonate 1000 MG (calcium 400 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".