NDC 69070-001 Shao Lin Pain Relief Plaster
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69070 - Zhejiang Dingtai Pharmaceutical Co.; Ltd
- 69070-001 - Shao Lin Pain Relief Plaster
Product Packages
NDC Code 69070-001-05
Package Description: 5 PATCH in 1 BOX / 1 g in 1 PATCH
Product Details
What is NDC 69070-001?
What are the uses for Shao Lin Pain Relief Plaster?
Which are Shao Lin Pain Relief Plaster UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Shao Lin Pain Relief 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)
- LINDERA AGGREGATA ROOT (UNII: 517Q7XRT2T)
- BLETILLA STRIATA BULB (UNII: 00T5SH6SEJ)
- ANGELICA DAHURICA ROOT (UNII: 1V63N2S972)
- AMPELOPSIS JAPONICA ROOT (UNII: O2672197TF)
- PAWPAW (UNII: 8P95FP65YO)
- SPARGANIUM STOLONIFERUM WHOLE (UNII: 873IV8AW3C)
- CURCUMA ZEDOARIA LEAF (UNII: M9E9LQH7N4)
- ANGELICA SINENSIS ROOT (UNII: B66F4574UG)
- PAEONIA VEITCHII ROOT (UNII: VX6GD6M93V)
- CINNAMON (UNII: 5S29HWU6QB)
- RHEUM PALMATUM WHOLE (UNII: 75P857ARCY)
- FORSYTHIA SUSPENSA WHOLE (UNII: RO2K2K561Z)
- DRAGON'S BLOOD (UNII: M3YJ2C28IC)
- FRANKINCENSE (UNII: R9XLF1R1WM)
- MYRRH (UNII: JC71GJ1F3L)
- PANAX NOTOGINSENG ROOT (UNII: GQX1C1175U)
- ACACIA CATECHU WHOLE (UNII: TJ6XA84OQF)
- BORNEOL (UNII: M89NIB437X)
What is the NDC to RxNorm Crosswalk for Shao Lin Pain Relief Plaster?
- RxCUI: 1650234 - menthol 5 % / methyl salicylate 5 % Medicated Patch
- RxCUI: 1650234 - menthol 0.05 MG/MG / methyl salicylate 0.05 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".