NDC 50462-115 Noble Lion Medicated Balm
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50462 - Abbp (arrington, Battle, Bell & Perry), Llc
- 50462-115 - Noble Lion Medicated Balm
Product Packages
NDC Code 50462-115-05
Package Description: 1 BOTTLE in 1 CARTON / 15 mL in 1 BOTTLE
NDC Code 50462-115-11
Package Description: 1 BOTTLE in 1 CARTON / 30 mL in 1 BOTTLE
NDC Code 50462-115-22
Package Description: 1 BOTTLE in 1 CARTON / 60 mL in 1 BOTTLE
Product Details
What is NDC 50462-115?
What are the uses for Noble Lion Medicated Balm?
Which are Noble Lion Medicated Balm UNII Codes?
The UNII codes for the active ingredients in this product are:
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- METHYL SALICYLATE (UNII: LAV5U5022Y) (Active Moiety)
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Noble Lion Medicated Balm 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:
- MINERAL OIL (UNII: T5L8T28FGP)
- ALCOHOL (UNII: 3K9958V90M)
- CORN OIL (UNII: 8470G57WFM)
- ROSA DAMASCENA FLOWER OIL (UNII: 18920M3T13)
What is the NDC to RxNorm Crosswalk for Noble Lion Medicated Balm?
- RxCUI: 1301423 - menthol 14.5 % / methyl salicylate 30 % Topical Ointment
- RxCUI: 1301423 - menthol 0.145 MG/MG / methyl salicylate 0.3 MG/MG Topical Ointment
- RxCUI: 1301428 - NOBLE LION Medicated Balm 14.5 % / 30 % Topical Ointment
- RxCUI: 1301428 - menthol 0.145 MG/MG / methyl salicylate 0.3 MG/MG Topical Ointment [Noble Lion Medicated Balm]
- RxCUI: 1301428 - Noble Lion Medicated Balm (menthol 14.5 % / methyl salicylate 30 % ) Topical Ointment
* 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".