NDC 14720-372 Double Prawn Brand Herbal Oil
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 14720 - Tai Tong Ah Co Pte Ltd
- 14720-372 - Double Prawn Brand Herbal Oil
Product Characteristics
Product Packages
NDC Code 14720-372-30
Package Description: 1 BOTTLE, GLASS in 1 CARTON / 28 mL in 1 BOTTLE, GLASS (14720-372-29)
Product Details
What is NDC 14720-372?
What are the uses for Double Prawn Brand Herbal Oil?
Which are Double Prawn Brand Herbal Oil UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Double Prawn Brand Herbal Oil 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:
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
- DICTAMNUS DASYCARPUS WHOLE (UNII: IM7ZCU30YH)
- COMMIPHORA MYRRHA WHOLE (UNII: UU81N77RI7)
- SOPHORA FLAVESCENS WHOLE (UNII: X8KX602M5L)
- SANGUISORBA OFFICINALIS WHOLE (UNII: J578M57Q8Z)
- GLEDITSIA SINENSIS WHOLE (UNII: FS3UB95UTG)
- RHEUM PALMATUM WHOLE (UNII: 75P857ARCY)
What is the NDC to RxNorm Crosswalk for Double Prawn Brand Herbal Oil?
- RxCUI: 1442685 - menthol 3.5 % Topical Oil
- RxCUI: 1442685 - menthol 35 MG/ML Topical Oil
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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".