NDC 36987-2234 Orris Root
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 36987-2234?
What are the uses for Orris Root?
Which are Orris Root UNII Codes?
The UNII codes for the active ingredients in this product are:
- COTTON (UNII: 7S4U9R5259)
- COTTON (UNII: 7S4U9R5259) (Active Moiety)
- COTTON FIBER (UNII: 70LDW53ROO)
- COTTON FIBER (UNII: 70LDW53ROO) (Active Moiety)
- COTTON SEED (UNII: DI0ZRJ0MXN)
- COTTON SEED (UNII: DI0ZRJ0MXN) (Active Moiety)
- FLAX SEED (UNII: 4110YT348C)
- FLAX SEED (UNII: 4110YT348C) (Active Moiety)
- CEIBA PENTANDRA FIBER (UNII: 758Z9H9WV9)
- CEIBA PENTANDRA FIBER (UNII: 758Z9H9WV9) (Active Moiety)
- IRIS GERMANICA VAR. FLORENTINA ROOT (UNII: M30XO5X4XD)
- IRIS GERMANICA VAR. FLORENTINA ROOT (UNII: M30XO5X4XD) (Active Moiety)
Which are Orris Root 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)
- PHENOL (UNII: 339NCG44TV)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Orris Root?
- RxCUI: 1014199 - jute fiber allergenic extract 50 MG/mL Injectable Solution
- RxCUI: 1014199 - jute fiber allergenic extract 50 MG/ML Injectable Solution
- RxCUI: 1014199 - Corcorus capsularis fiber extract 0.05 GM/ML Injectable Solution
- RxCUI: 1014199 - Corcorus capsularis fiber extract 50 MG/ML Injectable Solution
- RxCUI: 1098356 - orris root allergenic 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".