NDC 42217-201 Shang Shi Zhi Tong Gao
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What is NDC 42217-201?
What are the uses for Shang Shi Zhi Tong Gao?
Which are Shang Shi 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)
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Shang Shi 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)
What is the NDC to RxNorm Crosswalk for Shang Shi Zhi Tong Gao?
- RxCUI: 1490792 - camphor 3 % / menthol 1.5 % / methyl salicylate 2.5 % Medicated Patch
- RxCUI: 1490792 - camphor 0.03 MG/MG / menthol 0.015 MG/MG / methyl salicylate 0.025 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".