NDC 55614-660 Neck And Lumbar Pain Relieving Balm
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 55614-660?
Which are Neck And Lumbar Pain Relieving Balm UNII Codes?
The UNII codes for the active ingredients in this product are:
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (Active Moiety)
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Neck And Lumbar Pain Relieving Balm 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:
- ANGELICA SINENSIS ROOT (UNII: B66F4574UG)
- BIANCAEA SAPPAN WOOD (UNII: 086263LQDD)
- CITRUS AURANTIUM FRUIT (UNII: DQD16J2B5O)
- CRASSOSTREA GIGAS SHELL (UNII: 5I0R0U8ZL0)
- CYATHULA OFFICINALIS ROOT (UNII: BRM37UP34O)
- DIPSACUS ASPER ROOT (UNII: LB1GQP4253)
- DRAGON'S BLOOD (UNII: M3YJ2C28IC)
- EUCOMMIA ULMOIDES BARK (UNII: L878N1L0AR)
- FRANKINCENSE (UNII: R9XLF1R1WM)
- LEONURUS JAPONICUS FLOWERING TOP (UNII: V315CCZ08Z)
- LIGUSTICUM SINENSE SUBSP. CHUANXIONG ROOT (UNII: RR83T99U97)
- MYRRH (UNII: JC71GJ1F3L)
- OLIVE OIL (UNII: 6UYK2W1W1E)
- PANAX NOTOGINSENG ROOT (UNII: GQX1C1175U)
- RUBIA CORDIFOLIA ROOT (UNII: 4V873H15CG)
- SAFFLOWER (UNII: 4VBL71TY4Y)
- SALVIA MILTIORRHIZA ROOT (UNII: 1693AM5SBN)
- SENEGALIA CATECHU WOOD (UNII: CHL342Y4LA)
- SPATHOLOBUS SUBERECTUS STEM (UNII: N51VZ363BA)
- TAXILLUS CHINENSIS TOP (UNII: QJ523LD71P)
- WHITE WAX (UNII: 7G1J5DA97F)
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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".