NDC 30142-312 Kroger Multi Symptom Antacid
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 30142 - Kroger Company
- 30142-312 - Kroger Multi Symptom
Product Characteristics
Product Packages
NDC Code 30142-312-00
Package Description: 100 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC
Product Details
What is NDC 30142-312?
What are the uses for Kroger Multi Symptom Antacid?
Which are Kroger Multi Symptom Antacid UNII Codes?
The UNII codes for the active ingredients in this product are:
- CALCIUM CARBONATE (UNII: H0G9379FGK)
- CALCIUM CATION (UNII: 2M83C4R6ZB) (Active Moiety)
- MAGNESIUM HYDROXIDE (UNII: NBZ3QY004S)
- MAGNESIUM CATION (UNII: T6V3LHY838) (Active Moiety)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE (UNII: 92RU3N3Y1O) (Active Moiety)
Which are Kroger Multi Symptom 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:
- STARCH, CORN (UNII: O8232NY3SJ)
- DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2)
- D&C RED NO. 27 (UNII: 2LRS185U6K)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SUCRALOSE (UNII: 96K6UQ3ZD4)
What is the NDC to RxNorm Crosswalk for Kroger Multi Symptom Antacid?
- RxCUI: 476553 - calcium carbonate 675 MG / magnesium hydroxide 135 MG / simethicone 60 MG Chewable Tablet
- RxCUI: 476553 - calcium carbonate 675 MG / milk of magnesia 135 MG / simethicone 60 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".