NDC 16597-4873 Lekon Herbal Patch Green
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 16597 - Taiwan Three Mast Pharmaceutical Company Limited
- 16597-4873 - Lekon Herbal Patch Green
Product Characteristics
Product Packages
NDC Code 16597-4873-4
Package Description: 10 PATCH in 1 BAG / 10 g in 1 PATCH
Product Details
What is NDC 16597-4873?
What are the uses for Lekon Herbal Patch Green?
Which are Lekon Herbal Patch Green UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (Active Moiety)
Which are Lekon Herbal Patch Green 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:
- ACONITUM CARMICHAELII ROOT (UNII: XJ28061U1S)
- ACONITUM KUSNEZOFFII ROOT (UNII: 3L29I4K8KX)
- REHMANNIA GLUTINOSA ROOT (UNII: 1BEM3U6LQQ)
- AMPELOPSIS JAPONICA ROOT (UNII: O2672197TF)
- BLETILLA STRIATA BULB (UNII: 00T5SH6SEJ)
- ANGELICA SINENSIS ROOT (UNII: B66F4574UG)
- ANGELICA DAHURICA ROOT (UNII: 1V63N2S972)
- PAEONIA LACTIFLORA ROOT (UNII: 3Z3866YW6P)
- NOTOPTERYGIUM FRANCHETII ROOT (UNII: KRT28P6ITK)
- SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K)
- LINDERA AGGREGATA ROOT (UNII: 517Q7XRT2T)
- LICORICE (UNII: 61ZBX54883)
- ANGELICA PUBESCENS ROOT (UNII: 0MF1EI01KJ)
- SCROPHULARIA NINGPOENSIS ROOT (UNII: HC0FB6P85R)
- RHEUM OFFICINALE ROOT (UNII: A47JP5ZG9M)
- SALIX BABYLONICA WHOLE (UNII: 629X19YOW6)
- ILEX PUBESCENS ROOT (UNII: V5V22LFX73)
What is the NDC to RxNorm Crosswalk for Lekon Herbal Patch Green?
- RxCUI: 1599060 - camphor 3 % / menthol 5.1 % Medicated Patch
- RxCUI: 1599060 - camphor 0.03 MG/MG / menthol 0.051 MG/MG Medicated Patch
* 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".