NDC 61941-0234 Cold-eeze Gummies Plus Multi-symptom Relief Cold And Flu
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 61941 - Prophase Labs, Inc.
- 61941-0234 - Cold-eeze
Product Characteristics
Product Packages
NDC Code 61941-0234-0
Package Description: 36 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC
Product Details
What is NDC 61941-0234?
What are the uses for Cold-eeze Gummies Plus Multi-symptom Relief Cold And Flu?
Which are Cold-eeze Gummies Plus Multi-symptom Relief Cold And Flu UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC GLUCONATE (UNII: U6WSN5SQ1Z)
- ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)
- MENTHA PIPERITA (UNII: 79M2M2UDA9)
- MENTHA PIPERITA (UNII: 79M2M2UDA9) (Active Moiety)
- EUPATORIUM PERFOLIATUM FLOWERING TOP (UNII: 1W0775VX6E)
- EUPATORIUM PERFOLIATUM FLOWERING TOP (UNII: 1W0775VX6E) (Active Moiety)
- SAMBUCUS NIGRA FLOWER (UNII: 07V4DX094T)
- SAMBUCUS NIGRA FLOWER (UNII: 07V4DX094T) (Active Moiety)
- MYRRH (UNII: JC71GJ1F3L)
- MYRRH (UNII: JC71GJ1F3L) (Active Moiety)
- GLYCYRRHIZA GLABRA LEAF (UNII: GH32M797Y9)
- GLYCYRRHIZA GLABRA LEAF (UNII: GH32M797Y9) (Active Moiety)
Which are Cold-eeze Gummies Plus Multi-symptom Relief Cold And Flu 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:
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- CORN SYRUP (UNII: 9G5L16BK6N)
- GELATIN, UNSPECIFIED (UNII: 2G86QN327L)
- GLYCINE (UNII: TE7660XO1C)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- PECTIN (UNII: 89NA02M4RX)
- SUCROSE (UNII: C151H8M554)
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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".