NDC 49795-416 Professional Therapy Muscle Care Pain Relieving Gel By Dr. Chris Oswald Maximum Strength
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 49795 - Nutri-dyn Products Ltd. Dba Professional Health Products
- 49795-416 - Professional Therapy Muscle Care Pain Relieving Gel By Dr. Chris Oswald
Product Packages
NDC Code 49795-416-85
Package Description: 85 g in 1 TUBE, WITH APPLICATOR
Product Details
What is NDC 49795-416?
Which are Professional Therapy Muscle Care Pain Relieving Gel By Dr. Chris Oswald Maximum Strength UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
- CAMPHOR (UNII: 5TJD82A1ET)
- CAMPHOR (UNII: 5TJD82A1ET) (Active Moiety)
Which are Professional Therapy Muscle Care Pain Relieving Gel 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)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- PEPPERMINT OIL (UNII: AV092KU4JH)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- GLYCERIN (UNII: PDC6A3C0OX)
- DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
- GLUCOSAMINE SULFATE (UNII: 1FW7WLR731)
- MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
What is the NDC to RxNorm Crosswalk for Professional Therapy Muscle Care Pain Relieving Gel By Dr. Chris Oswald Maximum Strength?
- RxCUI: 1039731 - camphor 4 % / menthol 10 % Topical Gel
- RxCUI: 1039731 - camphor 0.04 MG/MG / menthol 0.1 MG/MG Topical Gel
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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".