NDC 72963-003 She Xiang Zhuang Gu Gao Regular
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 72963 - Inner Mongolia Horqin Pharmaceutical Co., Ltd
- 72963-003 - She Xiang Zhuang Gu Gao Regular
Product Packages
NDC Code 72963-003-10
Package Description: 10 PATCH in 1 BOX / 2.98 g in 1 PATCH
Product Details
What is NDC 72963-003?
What are the uses for She Xiang Zhuang Gu Gao Regular?
Which are She Xiang Zhuang Gu Gao Regular 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 Regular 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 Regular?
- 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
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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".