NDC 61941-0225 Cold-eeze Daytime And Nighttime Quickmelts
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
BLUE (C48333)
PM
Code Structure Chart
Product Details
What is NDC 61941-0225?
What are the uses for Cold-eeze Daytime And Nighttime Quickmelts?
Which are Cold-eeze Daytime And Nighttime Quickmelts UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC GLUCONATE (UNII: U6WSN5SQ1Z)
- ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)
- VALERIAN (UNII: JWF5YAW3QW)
- VALERIAN (UNII: JWF5YAW3QW) (Active Moiety)
- CHAMOMILE (UNII: FGL3685T2X)
- CHAMOMILE (UNII: FGL3685T2X) (Active Moiety)
Which are Cold-eeze Daytime And Nighttime Quickmelts 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:
- GLYCINE (UNII: TE7660XO1C)
- MALIC ACID (UNII: 817L1N4CKP)
- CROSPOVIDONE (UNII: 68401960MK)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- MANNITOL (UNII: 3OWL53L36A)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
- STEVIA REBAUDIUNA LEAF (UNII: 6TC6NN0876)
- SUCRALOSE (UNII: 96K6UQ3ZD4)
- TALC (UNII: 7SEV7J4R1U)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
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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".