NDC 49035-103 Equate Ultra Strength Antacid Calcium Carbonate 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 49035-103?
What are the uses for Equate Ultra Strength Antacid Calcium Carbonate Assorted Fruit?
Which are Equate Ultra Strength Antacid Calcium Carbonate 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 Equate Ultra Strength Antacid Calcium Carbonate 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)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- DEXTROSE (UNII: IY9XDZ35W2)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- D&C RED NO. 27 (UNII: 2LRS185U6K)
- STARCH, CORN (UNII: O8232NY3SJ)
- SUCRALOSE (UNII: 96K6UQ3ZD4)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
What is the NDC to RxNorm Crosswalk for Equate Ultra Strength Antacid Calcium Carbonate 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".