NDC 64762-874 Nbe Cherry Cold Remedy Fast Melting (rite Aid)
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
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Product Details
What is NDC 64762-874?
What are the uses for Nbe Cherry Cold Remedy Fast Melting (rite Aid)?
Which are Nbe Cherry Cold Remedy Fast Melting (rite Aid) UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC ACETATE (UNII: FM5526K07A)
- ZINC (UNII: J41CSQ7QDS) (Active Moiety)
- ZINC GLUCONATE (UNII: U6WSN5SQ1Z)
Which are Nbe Cherry Cold Remedy Fast Melting (rite Aid) 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:
- COPOVIDONE (UNII: D9C330MD8B)
- CROSPOVIDONE (UNII: 68401960MK)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- MANNITOL (UNII: 3OWL53L36A)
- GLYCYRRHIZIN, AMMONIATED (UNII: 3VRD35U26C)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
- SORBITOL (UNII: 506T60A25R)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- SUCRALOSE (UNII: 96K6UQ3ZD4)
* Please review the disclaimer below.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
[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".