NDC 61821-052 Dieda Fengshi Gao Medicated
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What is NDC 61821-052?
What are the uses for Dieda Fengshi Gao Medicated?
Which are Dieda Fengshi Gao Medicated 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)
- MENTHYL SALICYLATE, (+/-)- (UNII: 43XOA705ZD)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Dieda Fengshi Gao Medicated 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:
- OCIMUM GRATISSIMUM WHOLE (UNII: 7V3N80T4VS)
- CINNAMON OIL (UNII: E5GY4I6YCZ)
- SAPOSHNIKOVIA DIVARICATA ROOT (UNII: 8H84LFK2QD)
- LIQUIDAMBAR FORMOSANA RESIN (UNII: 597LBL467J)
- GREATER GALANGAL (UNII: 7Y64R856MB)
- GINGER (UNII: C5529G5JPQ)
- GLECHOMA LONGITUBA TOP (UNII: D352074L9S)
- NATURAL LATEX RUBBER (UNII: 2LQ0UUW8IN)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919)
- ROSIN (UNII: 88S87KL877)
- SAFFLOWER (UNII: 4VBL71TY4Y)
- SCHIZONEPETA TENUIFOLIA FLOWERING TOP (UNII: 2FN3BA1MZE)
What is the NDC to RxNorm Crosswalk for Dieda Fengshi Gao Medicated?
- RxCUI: 1429374 - camphor 8.3 % / menthol 3.32 % / methyl salicylate 13.84 % Medicated Patch
- RxCUI: 1429374 - camphor 0.083 MG/MG / menthol 0.0332 MG/MG / methyl salicylate 0.138 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".