NDC 13411-843 Legend Premium Heartburn Relief - Extra Strength Chewable
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 13411 - Advanced Pharmaceutical Services, Inc. Dba Affordable Quality Pharmaceuticals
- 13411-843 - Legend Premium Heartburn Relief - Extra Strength Chewable
Product Characteristics
Product Packages
NDC Code 13411-843-24
Package Description: 24 TABLET in 1 BOX
NDC Code 13411-843-30
Package Description: 30 TABLET in 1 BOX
NDC Code 13411-843-60
Package Description: 60 TABLET in 1 BOX
Product Details
What is NDC 13411-843?
What are the uses for Legend Premium Heartburn Relief - Extra Strength Chewable?
Which are Legend Premium Heartburn Relief - Extra Strength Chewable 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 Legend Premium Heartburn Relief - Extra Strength Chewable 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:
- DEXTROSE MONOHYDRATE (UNII: LX22YL083G)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- SUCROSE (UNII: C151H8M554)
- HOUTTUYNIA CORDATA FLOWERING TOP (UNII: RH041UUZ22)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- POVIDONE K30 (UNII: U725QWY32X)
- WATER (UNII: 059QF0KO0R)
- XYLITOL (UNII: VCQ006KQ1E)
- SORBITOL (UNII: 506T60A25R)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- PEPPERMINT (UNII: V95R5KMY2B)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
What is the NDC to RxNorm Crosswalk for Legend Premium Heartburn Relief - Extra Strength Chewable?
- 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
* Please review the disclaimer below.
[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".