NDC 68048-922 Shennong Analgesic Plaster
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 68048-922?
What are the uses for Shennong Analgesic Plaster?
Which are Shennong Analgesic Plaster 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 Shennong Analgesic 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:
- PANAX PSEUDOGINSENG ROOT (UNII: NMK0ZS613U)
- ANGELICA DAHURICA ROOT (UNII: 1V63N2S972)
- CIBOTIUM BAROMETZ ROOT (UNII: 2YP9JGT10R)
- NOTOPTERYGIUM INCISUM ROOT (UNII: 5Z2WW4J6RI)
- SAPOSHNIKOVIA DIVARICATA ROOT (UNII: 8H84LFK2QD)
- ACTAEA CIMICIFUGA ROOT (UNII: 65J267BAZT)
- SAFFLOWER (UNII: 4VBL71TY4Y)
- LIGUSTICUM WALLICHII ROOT (UNII: R81AD159QS)
- ANGELICA SINENSIS ROOT (UNII: B66F4574UG)
- MYRRH (UNII: JC71GJ1F3L)
- PARIS POLYPHYLLA WHOLE (UNII: 1E5W175DRX)
- FRANKINCENSE (UNII: R9XLF1R1WM)
- BASIL OIL (UNII: Z129UMU8LE)
- ATROPA BELLADONNA (UNII: WQZ3G9PF0H)
- NATURAL LATEX RUBBER (UNII: 2LQ0UUW8IN)
- ROSIN (UNII: 88S87KL877)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- PETROLATUM (UNII: 4T6H12BN9U)
- LANOLIN (UNII: 7EV65EAW6H)
What is the NDC to RxNorm Crosswalk for Shennong Analgesic Plaster?
- RxCUI: 1793754 - camphor 4.28 % / menthol 2.84 % / methyl salicylate 1.4 % Medicated Patch
- RxCUI: 1793754 - camphor 0.0428 MG/MG / menthol 0.0284 MG/MG / methyl salicylate 0.014 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".