NDC 49288-0259 Hog Hair
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 49288-0259?
What are the uses for Hog Hair?
Which are Hog Hair UNII Codes?
The UNII codes for the active ingredients in this product are:
- CANIS LUPUS FAMILIARIS HAIR (UNII: 05S7L91ZTR)
- CANIS LUPUS FAMILIARIS HAIR (UNII: 05S7L91ZTR) (Active Moiety)
- GALLUS GALLUS FEATHER (UNII: 1FCM16V0FV)
- GALLUS GALLUS FEATHER (UNII: 1FCM16V0FV) (Active Moiety)
- ANAS PLATYRHYNCHOS FEATHER (UNII: 83B65P4796)
- ANAS PLATYRHYNCHOS FEATHER (UNII: 83B65P4796) (Active Moiety)
- ANSER ANSER FEATHER (UNII: 15XI414745)
- ANSER ANSER FEATHER (UNII: 15XI414745) (Active Moiety)
- BOS TAURUS HAIR (UNII: TOQ97Z8644)
- BOS TAURUS HAIR (UNII: TOQ97Z8644) (Active Moiety)
- CAVIA PORCELLUS HAIR (UNII: KBA5Y6X57N)
- CAVIA PORCELLUS HAIR (UNII: KBA5Y6X57N) (Active Moiety)
- ORYCTOLAGUS CUNICULUS HAIR (UNII: 09N62XQ70Y)
- ORYCTOLAGUS CUNICULUS HAIR (UNII: 09N62XQ70Y) (Active Moiety)
- SUS SCROFA HAIR (UNII: 7Q7T9Z7QUW)
- SUS SCROFA HAIR (UNII: 7Q7T9Z7QUW) (Active Moiety)
Which are Hog Hair 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:
- GLYCERIN (UNII: PDC6A3C0OX)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM BICARBONATE (UNII: 8MDF5V39QO)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Hog Hair?
- RxCUI: 892854 - duck feather extract 50 MG/mL Injectable Solution
- RxCUI: 892854 - duck feather extract 50 MG/ML Injectable Solution
- RxCUI: 892854 - Anas platyrhynchos feather extract 0.05 GM/ML Injectable Solution
- RxCUI: 892854 - Anas platyrhynchos feather extract 1 GM per 20 ML Injectable Solution
- RxCUI: 892854 - Anas platyrhynchos feather extract 50 MG/ML Injectable Solution
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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".