NDC 14720-371 Double Prawn Rumagon
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 14720 - Tai Tong Ah Co., Pte. Ltd.
- 14720-371 - Double Prawn Rumagon
Product Packages
NDC Code 14720-371-28
Package Description: 12 BOX in 1 CARTON / 1 BOTTLE, GLASS in 1 BOX / 28 mL in 1 BOTTLE, GLASS
Product Details
What is NDC 14720-371?
What are the uses for Double Prawn Rumagon?
Which are Double Prawn Rumagon UNII Codes?
The UNII codes for the active ingredients in this product are:
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- METHYL SALICYLATE (UNII: LAV5U5022Y) (Active Moiety)
- TURPENTINE (UNII: XJ6RUH0O4G)
- TURPENTINE (UNII: XJ6RUH0O4G) (Active Moiety)
Which are Double Prawn Rumagon 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:
- CITRONELLA OIL (UNII: QYO8Q067D0)
What is the NDC to RxNorm Crosswalk for Double Prawn Rumagon?
- RxCUI: 1111078 - methyl salicylate 60 % / turpentine 24 % Topical Solution
- RxCUI: 1111078 - methyl salicylate 600 MG/ML / turpentine 240 MG/ML Topical Solution
- RxCUI: 1111082 - RUMAGON 60 % / 24 % Topical Solution
- RxCUI: 1111082 - methyl salicylate 600 MG/ML / turpentine 240 MG/ML Topical Solution [Rumagon]
- RxCUI: 1111082 - Rumagon (methyl salicylate 60 % / turpentine 24 % ) Topical Solution
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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".