NDC 65808-024 Cold And Flu Relief
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 65808 - Gmp Laboratories Of America, Inc
- 65808-024 - Cold And Flu Relief
Product Characteristics
Product Packages
NDC Code 65808-024-01
Package Description: 6 BLISTER PACK in 1 CARTON / 10 TABLET in 1 BLISTER PACK
Product Details
What is NDC 65808-024?
What are the uses for Cold And Flu Relief?
Which are Cold And Flu Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- ACONITUM NAPELLUS (UNII: U0NQ8555JD)
- ACONITUM NAPELLUS (UNII: U0NQ8555JD) (Active Moiety)
- ONION (UNII: 492225Q21H)
- ONION (UNII: 492225Q21H) (Active Moiety)
- GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q)
- GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (Active Moiety)
- JUSTICIA ADHATODA LEAF (UNII: HH159XOV81)
- JUSTICIA ADHATODA LEAF (UNII: HH159XOV81) (Active Moiety)
- POTASSIUM CHROMATE (UNII: 5P0R38CN2X)
- POTASSIUM CATION (UNII: 295O53K152) (Active Moiety)
- PULSATILLA VULGARIS (UNII: I76KB35JEV)
- PULSATILLA VULGARIS (UNII: I76KB35JEV) (Active Moiety)
- SANGUINARIA CANADENSIS ROOT (UNII: N9288CD508)
- SANGUINARIA CANADENSIS ROOT (UNII: N9288CD508) (Active Moiety)
- LOBARIA PULMONARIA (UNII: D1YM0P5Z2T)
- LOBARIA PULMONARIA (UNII: D1YM0P5Z2T) (Active Moiety)
- CAMPHOR (NATURAL) (UNII: N20HL7Q941)
- CAMPHOR (NATURAL) (UNII: N20HL7Q941) (Active Moiety)
Which are Cold And Flu Relief 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:
- POWDERED CELLULOSE (UNII: SMD1X3XO9M)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- DEXTROSE (UNII: IY9XDZ35W2)
- LACTOSE (UNII: J2B2A4N98G)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
* 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".