NDC 51367-014 Back Pain Relieving Oil
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 51367 - International Nature Nutraceuticals
- 51367-014 - Back Pain Relieving Oil
Product Packages
NDC Code 51367-014-40
Package Description: 1 OIL in 1 BOTTLE
Product Details
What is NDC 51367-014?
What are the uses for Back Pain Relieving Oil?
Which are Back Pain Relieving Oil UNII Codes?
The UNII codes for the active ingredients in this product are:
- CAMPHOR (NATURAL) (UNII: N20HL7Q941)
- CAMPHOR (NATURAL) (UNII: N20HL7Q941) (Active Moiety)
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Back Pain Relieving Oil 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 NOTOGINSENG ROOT (UNII: GQX1C1175U)
- DRAGON'S BLOOD (UNII: M3YJ2C28IC)
- ANGELICA SINENSIS ROOT (UNII: B66F4574UG)
- SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S)
- MYRRH (UNII: JC71GJ1F3L)
- FRANKINCENSE (UNII: R9XLF1R1WM)
- ANGELICA BISERRATA ROOT (UNII: OJ90180B22)
- CITRONELLA OIL (UNII: QYO8Q067D0)
- NOTOPTERYGIUM INCISUM ROOT (UNII: 5Z2WW4J6RI)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
What is the NDC to RxNorm Crosswalk for Back Pain Relieving Oil?
- RxCUI: 1441310 - camphor 9 % / menthol 11 % / methyl salicylate 17 % Topical Oil
- RxCUI: 1441310 - camphor 90 MG/ML / menthol 110 MG/ML / methyl salicylate 170 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".