NDC 49288-0582 Leaf Tobacco
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 49288-0582?
What are the uses for Leaf Tobacco?
Which are Leaf Tobacco UNII Codes?
The UNII codes for the active ingredients in this product are:
- COTTON FIBER (UNII: 70LDW53ROO)
- COTTON FIBER (UNII: 70LDW53ROO) (Active Moiety)
- CORCORUS CAPSULARIS FIBER (UNII: TVA75O7S63)
- CORCORUS CAPSULARIS FIBER (UNII: TVA75O7S63) (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)
- PYRETHRUM CINERARIIFOLIUM (UNII: CGF76TP7X6)
- PYRETHRUM CINERARIIFOLIUM (UNII: CGF76TP7X6) (Active Moiety)
- TOBACCO LEAF (UNII: 6YR2608RSU)
- TOBACCO LEAF (UNII: 6YR2608RSU) (Active Moiety)
Which are Leaf Tobacco 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 Leaf Tobacco?
- 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
* Please review the disclaimer below.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[6] What is the FDA Application Number? - This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
[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".