NDC 51367-003 Shao Lin Gao Pain Relieving Plaster
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 51367 - International Nature Nutraceuticals
- 51367-003 - Shao Lin Gao Pain Relieving Plaster
Product Packages
NDC Code 51367-003-08
Package Description: 8 PLASTER in 1 BOX
Product Details
What is NDC 51367-003?
What are the uses for Shao Lin Gao Pain Relieving Plaster?
Which are Shao Lin 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 Shao Lin 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:
- MUSTARD SEED (UNII: 58RXI817UT)
- ACHYRANTHES BIDENTATA ROOT (UNII: 5QIU26R6P1)
- DRYNARIA FORTUNEI ROOT (UNII: 731W842X8Q)
- FALLOPIA MULTIFLORA ROOT (UNII: AUZ3VD75MC)
- CHAENOMELES SINENSIS FRUIT (UNII: 6S5Q1Q537Z)
- DIPSACUS ASPER ROOT (UNII: LB1GQP4253)
- EUPATORIUM JAPONICUM WHOLE (UNII: 3M2V7JF1WO)
- ZEDOARY (UNII: 123C43G128)
- ELEUTHEROCOCCUS NODIFLORUS ROOT BARK (UNII: W7PRK433YB)
- PIPER KADSURA STEM (UNII: 80IOP41EL7)
- JUSTICIA GENDARUSSA LEAF (UNII: VBB21LWN1P)
- PARIS POLYPHYLLA ROOT (UNII: J4769SN11Q)
- PLATYCODON GRANDIFLORUM ROOT (UNII: 2DF0NS0O2Z)
- RHUBARB (UNII: G280W4MW6E)
- ANGELICA PUBESCENS ROOT (UNII: 0MF1EI01KJ)
- EUCOMMIA ULMOIDES BARK (UNII: L878N1L0AR)
- SAFFLOWER (UNII: 4VBL71TY4Y)
- REHMANNIA GLUTINOSA ROOT (UNII: 1BEM3U6LQQ)
What is the NDC to RxNorm Crosswalk for Shao Lin Gao Pain Relieving Plaster?
- RxCUI: 1304079 - camphor 21.21 MG / menthol 14.14 MG / methyl salicylate 64.45 MG Medicated Patch
- RxCUI: 1304079 - camphor 21.2 MG / menthol 14.1 MG / methyl salicylate 64.5 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".