NDC 21695-440 Banalg
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What is NDC 21695-440?
What are the uses for Banalg?
Which are Banalg 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 Banalg 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:
- 1,3-DIMETHYLBUTYL SALICYLATE (UNII: 47OL39K42M)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Banalg?
- RxCUI: 311506 - menthol 3 % / methyl salicylate 14 % Topical Lotion
- RxCUI: 311506 - menthol 30 MG/ML / methyl salicylate 140 MG/ML Topical Lotion
- RxCUI: 702415 - Banalg 3 % / 14 % Topical Lotion
- RxCUI: 702415 - menthol 30 MG/ML / methyl salicylate 140 MG/ML Topical Lotion [Banalg]
- RxCUI: 702415 - Banalg (menthol 3 % / methyl salicylate 14 % ) Topical Lotion
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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".