NDC 62209-9266 Huo Pao Tieh Ta Feng Shin Kao
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 62209 - Dah Wei Biochemical Pharmaceutic International Ltd.
- 62209-9266 - Huo Pao Tieh Ta Feng Shin Kao
Product Characteristics
Product Packages
NDC Code 62209-9266-5
Package Description: 6 PATCH in 1 BAG / 5 g in 1 PATCH
Product Details
What is NDC 62209-9266?
What are the uses for Huo Pao Tieh Ta Feng Shin Kao?
Which are Huo Pao Tieh Ta Feng Shin Kao UNII Codes?
The UNII codes for the active ingredients in this product are:
- LEVOMENTHOL (UNII: BZ1R15MTK7)
- LEVOMENTHOL (UNII: BZ1R15MTK7) (Active Moiety)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (Active Moiety)
Which are Huo Pao Tieh Ta Feng Shin Kao 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:
- SESAME OIL (UNII: QX10HYY4QV)
- MYRRH (UNII: JC71GJ1F3L)
- REHMANNIA GLUTINOSA WHOLE (UNII: 37S3F886KQ)
- ANGELICA DAHURICA WHOLE (UNII: 667W6C5J4P)
- ANGELICA SINENSIS WHOLE (UNII: 697D19QDBN)
- PAEONIA LACTIFLORA WHOLE (UNII: N44H57P7WG)
- NOTOPTERYGIUM INCISUM WHOLE (UNII: N8519Y5E6X)
- BLETILLA STRIATA WHOLE (UNII: WV2BSG60EW)
- LINDERA AGGREGATA WHOLE (UNII: 3ZU402829L)
- GLYCYRRHIZA URALENSIS (UNII: 42B5YD8F0K)
- ANGELICA PUBESCENS WHOLE (UNII: SV5CN7O3MB)
- SCROPHULARIA NINGPOENSIS WHOLE (UNII: 2FW4P6X3W8)
- RHEUM PALMATUM WHOLE (UNII: 75P857ARCY)
- CINNAMOMUM AROMATICUM WHOLE (UNII: 9BPF21T8ZR)
- MENTHA ARVENSIS WHOLE (UNII: 46477RRB3O)
What is the NDC to RxNorm Crosswalk for Huo Pao Tieh Ta Feng Shin Kao?
- RxCUI: 1490791 - camphor 40 MG / levomenthol 200 MG Medicated Patch
- RxCUI: 1490791 - camphor 0.008 MG/MG / levomenthol 0.04 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".