NDC 72963-002 Xiao Zhong Gao
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 72963 - Inner Mongolia Horqin Pharmaceutical Co., Ltd
- 72963-002 - Xiao Zhong Gao
Product Packages
NDC Code 72963-002-02
Package Description: 10 PATCH in 1 BOX / 1.3 g in 1 PATCH
Product Details
What is NDC 72963-002?
What are the uses for Xiao Zhong Gao?
Which are Xiao Zhong 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 Xiao Zhong 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:
- RHEUM OFFICINALE ROOT (UNII: A47JP5ZG9M)
- EUPHORBIA PEKINENSIS ROOT (UNII: 09S6R05TRN)
- POTENTILLA DISCOLOR WHOLE (UNII: T560PLD2E7)
- TURMERIC (UNII: 856YO1Z64F)
- ACORUS CALAMUS ROOT (UNII: XY1K7KIQ0F)
- ASPARAGUS COCHINCHINENSIS TUBER (UNII: IZW9WN28HW)
- POLYGONATUM ODORATUM ROOT (UNII: KPF03O64AZ)
- BORNEOL (UNII: M89NIB437X)
- NATURAL LATEX RUBBER (UNII: 2LQ0UUW8IN)
- ROSIN (UNII: 88S87KL877)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- PETROLATUM (UNII: 4T6H12BN9U)
- LANOLIN (UNII: 7EV65EAW6H)
- PARAFFIN (UNII: I9O0E3H2ZE)
- COCONUT OIL (UNII: Q9L0O73W7L)
What is the NDC to RxNorm Crosswalk for Xiao Zhong Gao?
- RxCUI: 2120574 - camphor 1.22 % / Capsicum extract 2.44 % / methyl salicylate 2.44 % Medicated Patch
- RxCUI: 2120574 - camphor 0.0122 MG/MG / menthol 0.0244 MG/MG / methyl salicylate 0.0244 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".