NDC 70692-118 Antacid Regular Strength
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
GREEN (C48329)
PINK (C48328 - REDDISH PINK)
ORANGE (C48331)
Code Structure Chart
Product Details
What is NDC 70692-118?
What are the uses for Antacid Regular Strength?
Which are Antacid Regular Strength 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 Antacid Regular Strength 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:
- SUCROSE (UNII: C151H8M554)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- ADIPIC ACID (UNII: 76A0JE0FKJ)
- MODIFIED CORN STARCH (1-OCTENYL SUCCINIC ANHYDRIDE) (UNII: 461P5CJN6T)
- CROSPOVIDONE (UNII: 2S7830E561)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- D&C RED NO. 30 (UNII: 2S42T2808B)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- FOOD YELLOW 3 FREE ACID (UNII: G2B7JWK1GG)
- DEXTROSE (UNII: IY9XDZ35W2)
- D&C RED NO. 27 (UNII: 2LRS185U6K)
- TALC (UNII: 7SEV7J4R1U)
What is the NDC to RxNorm Crosswalk for Antacid Regular Strength?
- RxCUI: 308907 - calcium carbonate 500 MG (Ca 200 MG) Chewable Tablet
- RxCUI: 308907 - calcium carbonate 500 MG Chewable Tablet
- RxCUI: 308907 - calcium carbonate 500 MG (equivalent to calcium 200 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".