NDC 75979-1146 Imbue Pain Relief
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 75979-1146?
What are the uses for Imbue Pain Relief?
Which are Imbue Pain Relief 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 Imbue Pain Relief 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:
- ACORUS GRAMINEUS ROOT (UNII: Z60N6Q6E19)
- ANGELICA SINENSIS ROOT (UNII: B66F4574UG)
- ARTEMISIA ARGYI LEAF (UNII: 2JYC99Q0WZ)
- ATRACTYLODES LANCEA ROOT (UNII: CAZ6282J2O)
- SESAME OIL (UNII: QX10HYY4QV)
- FRANKINCENSE (UNII: R9XLF1R1WM)
- SAFFLOWER (UNII: 4VBL71TY4Y)
- CINNAMON (UNII: 5S29HWU6QB)
- CNIDIUM MONNIERI FRUIT (UNII: V1IA3S3CUS)
- MYRRH (UNII: JC71GJ1F3L)
- CYATHULA OFFICINALIS ROOT (UNII: BRM37UP34O)
- WEST INDIAN LEMONGRASS OIL (UNII: 5BIA40E9ED)
- HELICHRYSUM ITALICUM FLOWER OIL (UNII: O97ZV7726K)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- LIGUSTICUM SINENSE SUBSP. CHUANXIONG ROOT (UNII: RR83T99U97)
- PAEONIA LACTIFLORA ROOT (UNII: 3Z3866YW6P)
- SAUSSUREA COSTUS ROOT (UNII: RUP970CGR9)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- DIOSCOREA COLLETTII VAR. HYPOGLAUCA ROOT (UNII: N57RVD5L6U)
- DRYNARIA FORTUNEI ROOT (UNII: 731W842X8Q)
- FLICKINGERIA FIMBRIATA STEM (UNII: D6E4A8IAEP)
- GENTIANA MACROPHYLLA ROOT (UNII: 6559FC0U1B)
- PINELLIA TERNATA ROOT (UNII: G9AET085M5)
- PINUS MASSONIANA RESIN (UNII: 64S07U83T7)
- ROSIN (UNII: 88S87KL877)
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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".