NDC 51367-004 Yao Shen Gao Pain Relieving Plaster
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What is NDC 51367-004?
What are the uses for Yao Shen Gao Pain Relieving Plaster?
Which are Yao Shen Gao Pain Relieving Plaster 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 Yao Shen Gao Pain Relieving Plaster 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 FRUIT (UNII: CK15HA8438)
- REHMANNIA GLUTINOSA ROOT (UNII: 1BEM3U6LQQ)
- CULLEN CORYLIFOLIUM FRUIT (UNII: 78AD6Z52S6)
- EPIMEDIUM GRANDIFLORUM WHOLE (UNII: S57NI79KGP)
- CNIDIUM MONNIERI FRUIT (UNII: V1IA3S3CUS)
- ACHYRANTHES BIDENTATA ROOT (UNII: 5QIU26R6P1)
- DIPSACUS ASPER ROOT (UNII: LB1GQP4253)
- LICORICE (UNII: 61ZBX54883)
- EUCOMMIA ULMOIDES BARK (UNII: L878N1L0AR)
- CUSCUTA CHINENSIS SEED (UNII: 77SZY178UD)
- LYCIUM BARBARUM FRUIT (UNII: 930626MWDL)
- PLANTAGO MAJOR SEED (UNII: YP0NFQ834U)
- FENNEL (UNII: 557II4LLC3)
- ACONITUM CARMICHAELII ROOT (UNII: XJ28061U1S)
- SCHISANDRA CHINENSIS FRUIT (UNII: ABS794681C)
- INDIAN FRANKINCENSE (UNII: 4PW41QCO2M)
- MYRRH (UNII: JC71GJ1F3L)
- SYZYGIUM AROMATICUM WHOLE (UNII: EY9MMA0P6Y)
- CHINESE CINNAMON OIL (UNII: A4WO0626T5)
- LIQUIDAMBAR STYRACIFLUA RESIN (UNII: P41GWD11CX)
- PETROLATUM (UNII: 4T6H12BN9U)
- LANOLIN (UNII: 7EV65EAW6H)
- CALCIUM CARBONATE (UNII: H0G9379FGK)
What is the NDC to RxNorm Crosswalk for Yao Shen Gao Pain Relieving Plaster?
- RxCUI: 1304085 - camphor 43.76 MG / menthol 37.02 MG / methyl salicylate 72.39 MG Medicated Patch
- RxCUI: 1304085 - camphor 43.8 MG / menthol 37 MG / methyl salicylate 72.4 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".