NDC 42217-203 Zhuang Gu She Xiang Zhi Tong Gao
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 42217 - Henan Lingrui Pharmaceutical Co.; Ltd
- 42217-203 - Zhuang Gu She Xiang Zhi Tong Gao
Product Packages
NDC Code 42217-203-10
Package Description: 10 PATCH in 1 BOX / 1 g in 1 PATCH
Product Details
What is NDC 42217-203?
What are the uses for Zhuang Gu She Xiang Zhi Tong Gao?
Which are Zhuang Gu She Xiang Zhi Tong Gao UNII Codes?
The UNII codes for the active ingredients in this product are:
- CAMPHOR (NATURAL) (UNII: N20HL7Q941)
- CAMPHOR (NATURAL) (UNII: N20HL7Q941) (Active Moiety)
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Zhuang Gu She Xiang Zhi Tong Gao 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:
- BOSWELLIA SACRA BARK (UNII: 1UK28DX728)
- COMMIPHORA MYRRHA TOP (UNII: N534J96ODY)
- CLOVE (UNII: K48IKT5321)
- CINNAMOMUM AROMATICUM WHOLE (UNII: 9BPF21T8ZR)
- SCHIZONEPETA TENUIFOLIA WHOLE (UNII: C1107616TR)
- SAPOSHNIKOVIA DIVARICATA ROOT (UNII: 8H84LFK2QD)
- GERANIUM WILFORDII TOP (UNII: 771B1S9W3R)
- PERIPLOCA SEPIUM ROOT BARK (UNII: 638OW484M3)
- DRYNARIA FORTUNEI ROOT (UNII: 731W842X8Q)
- ANGELICA DAHURICA ROOT (UNII: 1V63N2S972)
- GINGER (UNII: C5529G5JPQ)
- BORNEOL (UNII: M89NIB437X)
- BELLADONNA LEAF (UNII: 6GZW20TIOI)
- NATURAL LATEX RUBBER (UNII: 2LQ0UUW8IN)
- ROSIN (UNII: 88S87KL877)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- LANOLIN (UNII: 7EV65EAW6H)
- PARAFFIN (UNII: I9O0E3H2ZE)
- DIMETHYL SULFOXIDE (UNII: YOW8V9698H)
- ANTIOXIDANT 119 (UNII: UBL01213LI)
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- MUSK KETONE (UNII: 483V3E1L6J)
What is the NDC to RxNorm Crosswalk for Zhuang Gu She Xiang Zhi Tong Gao?
- RxCUI: 1489689 - camphor 3 % / menthol 2.9 % Medicated Patch
- RxCUI: 1489689 - camphor 0.03 MG/MG / menthol 0.029 MG/MG Medicated Patch
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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".