NDC 61079-014 Bb Medicated Pain Relieving Oil
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
YELLOW (C48330 - TRANSPARENT SLIGHT YELLOW COLORATION)
Code Structure Chart
Product Details
What is NDC 61079-014?
What are the uses for Bb Medicated Pain Relieving Oil?
Which are Bb Medicated Pain Relieving Oil UNII Codes?
The UNII codes for the active ingredients in this product are:
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (Active Moiety)
- LEVOMENTHOL (UNII: BZ1R15MTK7)
- LEVOMENTHOL (UNII: BZ1R15MTK7) (Active Moiety)
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- EUCALYPTUS OIL (UNII: 2R04ONI662) (Active Moiety)
- CAPSAICIN (UNII: S07O44R1ZM)
- CAPSAICIN (UNII: S07O44R1ZM) (Active Moiety)
- CAMPHOR (NATURAL) (UNII: N20HL7Q941)
- CAMPHOR (NATURAL) (UNII: N20HL7Q941) (Active Moiety)
Which are Bb Medicated 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:
- CETYL ALCOHOL (UNII: 936JST6JCN)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- SORBITAN MONOLAURATE (UNII: 6W9PS8B71J)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- ALCOHOL (UNII: 3K9958V90M)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Bb Medicated Pain Relieving Oil?
- RxCUI: 1598277 - camphor 3 % / capsaicin 0.25 % / eucalyptus oil 15 % / menthol 12 % / methyl salicylate 15 % Topical Oil
- RxCUI: 1598277 - camphor 30 MG/ML / capsaicin 2.5 MG/ML / Eucalyptus oil 150 MG/ML / menthol 120 MG/ML / methyl salicylate 150 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".