NDC 72963-001 She Xiang Zhuang Gu Gao
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 72963-001?
What are the uses for She Xiang Zhuang Gu Gao?
Which are She Xiang Zhuang Gu Gao UNII Codes?
The UNII codes for the active ingredients in this product are:
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (Active Moiety)
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are She Xiang Zhuang Gu 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:
- STAR ANISE (UNII: XKC1657P78)
- ANGELICA DAHURICA ROOT (UNII: 1V63N2S972)
- ATRACTYLODES LANCEA ROOT (UNII: CAZ6282J2O)
- ANGELICA SINENSIS ROOT (UNII: B66F4574UG)
- GINGER (UNII: C5529G5JPQ)
- CYNANCHUM PANICULATUM WHOLE (UNII: T14ONG8D7H)
- KAEMPFERIA GALANGA ROOT (UNII: 7B7U9D12AI)
- GERANIUM WILFORDII WHOLE (UNII: QXI974Y72W)
- CYATHULA OFFICINALIS ROOT (UNII: BRM37UP34O)
- MUSCONE (UNII: UPS3C6CV36)
- CHONDROITIN SULFATE (PORCINE) (UNII: V5E8ELO4W9)
- BORNEOL (UNII: M89NIB437X)
- DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40)
- NATURAL LATEX RUBBER (UNII: 2LQ0UUW8IN)
- ROSIN (UNII: 88S87KL877)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- PETROLATUM (UNII: 4T6H12BN9U)
- LANOLIN (UNII: 7EV65EAW6H)
- PARAFFIN (UNII: I9O0E3H2ZE)
What is the NDC to RxNorm Crosswalk for She Xiang Zhuang Gu Gao?
- RxCUI: 2120570 - camphor 1.91 % / menthol 2.54 % / methyl salicylate 1.62 % Medicated Patch
- RxCUI: 2120570 - camphor 0.0191 MG/MG / menthol 0.0254 MG/MG / methyl salicylate 0.0162 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".