NDC 49795-417 Professional Therapy Muscle Care Pain Relieving Ointment By Dr. Chris Oswald Maximum Strength
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 49795-417?
Which are Professional Therapy Muscle Care Pain Relieving Ointment By Dr. Chris Oswald Maximum Strength UNII Codes?
The UNII codes for the active ingredients in this product are:
- CAMPHOR (UNII: 5TJD82A1ET)
- CAMPHOR (UNII: 5TJD82A1ET) (Active Moiety)
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Professional Therapy Muscle Care Pain Relieving Ointment By Dr. Chris Oswald Maximum Strength 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:
- WATER (UNII: 059QF0KO0R)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- GLYCOL STEARATE (UNII: 0324G66D0E)
- DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
- GLYCERIN (UNII: PDC6A3C0OX)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- GLUCOSAMINE SULFATE (UNII: 1FW7WLR731)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- UREA (UNII: 8W8T17847W)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- VITAMIN E (UNII: H4N855PNZ1)
What is the NDC to RxNorm Crosswalk for Professional Therapy Muscle Care Pain Relieving Ointment By Dr. Chris Oswald Maximum Strength?
- RxCUI: 900390 - camphor 4 % / menthol 4 % Topical Ointment
- RxCUI: 900390 - camphor 0.04 MG/MG / menthol 0.04 MG/MG Topical Ointment
* Please review the disclaimer below.
[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".