NDC 13411-842 Legend Cough Lozenge
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 13411-842?
What are the uses for Legend Cough Lozenge?
Which are Legend Cough Lozenge UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Legend Cough Lozenge 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:
- HONEY (UNII: Y9H1V576FH)
- GINGER (UNII: C5529G5JPQ)
- LICORICE (UNII: 61ZBX54883)
- EUCALYPTOL (UNII: RV6J6604TK)
- PLECTRANTHUS AMBOINICUS WHOLE (UNII: T444G60821)
- CINNAMON OIL (UNII: E5GY4I6YCZ)
- MANNITOL (UNII: 3OWL53L36A)
- SORBITOL (UNII: 506T60A25R)
- POVIDONE K30 (UNII: U725QWY32X)
- XYLITOL (UNII: VCQ006KQ1E)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- ASPARTAME (UNII: Z0H242BBR1)
- SUCRALOSE (UNII: 96K6UQ3ZD4)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
What is the NDC to RxNorm Crosswalk for Legend Cough Lozenge?
- RxCUI: 199393 - menthol 10 MG Oral Lozenge
- RxCUI: 199393 - menthol 10 MG Oral Pastille
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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".