NDC 50845-0262 Vaccines
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
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Product Details
What is NDC 50845-0262?
What are the uses for Vaccines?
Which are Vaccines UNII Codes?
The UNII codes for the active ingredients in this product are:
- ARNICA MONTANA WHOLE (UNII: O80TY208ZW)
- ARNICA MONTANA (UNII: O80TY208ZW) (Active Moiety)
- HYPERICUM PERFORATUM WHOLE (UNII: XK4IUX8MNB)
- HYPERICUM PERFORATUM (UNII: XK4IUX8MNB) (Active Moiety)
- RHODODENDRON TOMENTOSUM LEAFY TWIG (UNII: 877L01IZ0P)
- LEDUM PALUSTRE TWIG (UNII: 877L01IZ0P) (Active Moiety)
- MEASLES VIRUS (UNII: HT3R7C012Q)
- MEASLES VIRUS (UNII: HT3R7C012Q) (Active Moiety)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- CHLORIDE ION (UNII: Q32ZN48698) (Active Moiety)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
- SULFUR IODIDE (UNII: L6L8KA2AA0)
- SULFUR IODIDE (UNII: L6L8KA2AA0) (Active Moiety)
- THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397)
- THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (Active Moiety)
- URTICA URENS WHOLE (UNII: IHN2NQ5OF9)
- URTICA URENS (UNII: IHN2NQ5OF9) (Active Moiety)
Which are Vaccines 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:
- WATER (UNII: 059QF0KO0R)
- ALCOHOL (UNII: 3K9958V90M)
* 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".