NDC 49288-0582 Leaf Tobacco
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 49288 - Antigen Laboratories, Inc.
- 49288-0582 - Leaf Tobacco
Product Packages
NDC Code 49288-0582-1
Package Description: 2 mL in 1 VIAL, MULTI-DOSE
NDC Code 49288-0582-2
Package Description: 5 mL in 1 VIAL, MULTI-DOSE
NDC Code 49288-0582-3
Package Description: 10 mL in 1 VIAL, MULTI-DOSE
NDC Code 49288-0582-4
Package Description: 30 mL in 1 VIAL, MULTI-DOSE
NDC Code 49288-0582-5
Package Description: 50 mL in 1 VIAL, MULTI-DOSE
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.
[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".