NDC 42217-205 Joint Analgesic Plaster
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 42217 - Henan Lingrui Pharmaceutical Co Ltd
- 42217-205 - Joint Analgesic Plaster
Product Packages
NDC Code 42217-205-10
Package Description: 10 PATCH in 1 BOX / 1 g in 1 PATCH
Product Details
What is NDC 42217-205?
What are the uses for Joint Analgesic Plaster?
Which are Joint 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)
Which are Joint 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:
- PEPPERS (UNII: T5KDM4J239)
- BELLADONNINE (UNII: 1DF50P9K2I)
- PEPPERMINT OIL (UNII: AV092KU4JH)
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- NIACIN (UNII: 2679MF687A)
- DIPHENHYDRAMINE (UNII: 8GTS82S83M)
- ROSIN (UNII: 88S87KL877)
- NATURAL LATEX RUBBER (UNII: 2LQ0UUW8IN)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- LANOLIN (UNII: 7EV65EAW6H)
- PETROLATUM (UNII: 4T6H12BN9U)
- PARAFFIN (UNII: I9O0E3H2ZE)
- ANTIOXIDANT 119 (UNII: UBL01213LI)
What is the NDC to RxNorm Crosswalk for Joint Analgesic Plaster?
- RxCUI: 1603829 - camphor 3 % Medicated Patch
- RxCUI: 1603829 - camphor 0.03 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".