NDC 53882-002 Stressa Back And Neck Pain Relieving
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 53882-002?
What are the uses for Stressa Back And Neck Pain Relieving?
Which are Stressa Back And Neck Pain Relieving UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Stressa Back And Neck Pain Relieving 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:
- ALMOND OIL (UNII: 66YXD4DKO9)
- APRICOT KERNEL OIL (UNII: 54JB35T06A)
- BASIL OIL (UNII: Z129UMU8LE)
- ARABICA COFFEE OIL (UNII: IK55HKE887)
- GALBANUM OIL (UNII: 211UF7M8N1)
- EUROPEAN HAZELNUT OIL (UNII: 8RQ2839AVG)
- HYSSOP OIL (UNII: 173D71924B)
- LEMON OIL (UNII: I9GRO824LL)
- NUTMEG OIL (UNII: Z1CLM48948)
- ROSEMARY OIL (UNII: 8LGU7VM393)
- SAGE OIL (UNII: U27K0H1H2O)
- PINE NEEDLE OIL (PINUS SYLVESTRIS) (UNII: 5EXL5H740Y)
- PICEA MARIANA LEAF OIL (UNII: Q1J49L1A5O)
- .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
- WHEAT GERM (UNII: YR3G369F5A)
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- CANANGA OIL (UNII: 8YOY78GNNX)
What is the NDC to RxNorm Crosswalk for Stressa Back And Neck Pain Relieving?
- RxCUI: 1545293 - menthol 1.25 % Topical Oil
- RxCUI: 1545293 - menthol 12.5 MG/ML Topical Oil
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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".