NDC 69406-001 Cedar Fever
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69406 - People's Pharmacy, Inc
- 69406-001 - Cedar Fever
Product Characteristics
Product Packages
NDC Code 69406-001-03
Package Description: 75 PELLET in 1 VIAL, GLASS
Product Details
What is NDC 69406-001?
What are the uses for Cedar Fever?
Which are Cedar Fever UNII Codes?
The UNII codes for the active ingredients in this product are:
- ONION (UNII: 492225Q21H)
- ONION (UNII: 492225Q21H) (Active Moiety)
- FRAXINUS AMERICANA BARK (UNII: 0B24UR1O1S)
- FRAXINUS AMERICANA BARK (UNII: 0B24UR1O1S) (Active Moiety)
- GALPHIMIA GLAUCA FLOWERING TOP (UNII: 93PH5Q8M7E)
- GALPHIMIA GLAUCA FLOWERING TOP (UNII: 93PH5Q8M7E) (Active Moiety)
- JUNIPERUS VIRGINIANA TWIG (UNII: 532BCG080L)
- JUNIPERUS VIRGINIANA TWIG (UNII: 532BCG080L) (Active Moiety)
- QUERCUS ROBUR TWIG BARK (UNII: 2JFK226947)
- QUERCUS ROBUR TWIG BARK (UNII: 2JFK226947) (Active Moiety)
- THUJA PLICATA LEAF (UNII: R9I752FESH)
- THUJA PLICATA LEAF (UNII: R9I752FESH) (Active Moiety)
- ULMUS RUBRA BARK (UNII: 91QY4PXU8Q)
- ULMUS RUBRA BARK (UNII: 91QY4PXU8Q) (Active Moiety)
Which are Cedar Fever 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:
- SUCROSE (UNII: C151H8M554)
- LACTOSE (UNII: J2B2A4N98G)
* 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".