NDC 22742-003 Shanghai Shang Shi Zhi Tong Gao Pain Relieving
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What is NDC 22742-003?
Which are Shanghai Shang Shi Zhi Tong Gao Pain Relieving 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 Shanghai Shang Shi Zhi Tong Gao Pain Relieving 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:
- CINNAMON (UNII: 5S29HWU6QB)
- CLOVE (UNII: K48IKT5321)
- DRYNARIA FORTUNEI ROOT (UNII: 731W842X8Q)
- SAPOSHNIKOVIA DIVARICATA ROOT (UNII: 8H84LFK2QD)
- ANGELICA DAHURICA ROOT (UNII: 1V63N2S972)
- FRANKINCENSE (UNII: R9XLF1R1WM)
- GERANIUM WILFORDII WHOLE (UNII: QXI974Y72W)
- ROSIN PARTIALLY DIMERIZED GLYCEROL ESTER (UNII: BY866DXY67)
- CENTELLA ASIATICA (UNII: 7M867G6T1U)
- ALPINIA GALANGA WHOLE (UNII: 3S1W839C0O)
- KAOLIN (UNII: 24H4NWX5CO)
- LANOLIN (UNII: 7EV65EAW6H)
- BARIUM SULFATE (UNII: 25BB7EKE2E)
- ZINC SULFIDE (UNII: KPS085631O)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- MINERAL OIL (UNII: T5L8T28FGP)
- MYRRH (UNII: JC71GJ1F3L)
- LIQUIDAMBAR ORIENTALIS WHOLE (UNII: 759QNU787E)
- PARAFFIN (UNII: I9O0E3H2ZE)
- PERIPLOCA SEPIUM ROOT BARK (UNII: 638OW484M3)
- PETROLATUM (UNII: 4T6H12BN9U)
- SCHIZONEPETA TENUIFOLIA WHOLE (UNII: C1107616TR)
What is the NDC to RxNorm Crosswalk for Shanghai Shang Shi Zhi Tong Gao Pain Relieving?
- RxCUI: 1733821 - camphor 10 % / menthol 10.28 % / methyl salicylate 15.43 % Medicated Patch
- RxCUI: 1733821 - camphor 0.1 MG/MG / menthol 0.103 MG/MG / methyl salicylate 0.154 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".