NDC 36987-2246 Jute
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Packages
NDC Code 36987-2246-1
Package Description: 5 mL in 1 VIAL, MULTI-DOSE
NDC Code 36987-2246-2
Package Description: 10 mL in 1 VIAL, MULTI-DOSE
NDC Code 36987-2246-3
Package Description: 30 mL in 1 VIAL, MULTI-DOSE
NDC Code 36987-2246-4
Package Description: 50 mL in 1 VIAL, MULTI-DOSE
Product Details
What is NDC 36987-2246?
What are the uses for Jute?
Which are Jute UNII Codes?
The UNII codes for the active ingredients in this product are:
- FLAX SEED (UNII: 4110YT348C)
- FLAX SEED (UNII: 4110YT348C) (Active Moiety)
- TOBACCO LEAF (UNII: 6YR2608RSU)
- TOBACCO LEAF (UNII: 6YR2608RSU) (Active Moiety)
- CORCORUS CAPSULARIS FIBER (UNII: TVA75O7S63)
- CORCORUS CAPSULARIS FIBER (UNII: TVA75O7S63) (Active Moiety)
Which are Jute 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:
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM BICARBONATE (UNII: 8MDF5V39QO)
- WATER (UNII: 059QF0KO0R)
- PHENOL (UNII: 339NCG44TV)
What is the NDC to RxNorm Crosswalk for Jute?
- RxCUI: 1014203 - jute fiber allergenic extract 10,000 UNT/mL Injectable Solution
- RxCUI: 1014203 - jute fiber allergenic extract 10000 UNT/ML Injectable Solution
- RxCUI: 1014203 - Corcorus capsularis fiber extract 10,000 UNT/ML Injectable Solution
- RxCUI: 1014203 - jute fiber extract 10,000 UNT/ML Injectable Solution
- RxCUI: 889596 - tobacco leaf allergenic extract 10,000 UNT/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".