NDC 76163-010 Dr.oh Patch
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 76163-010?
What are the uses for Dr.oh Patch?
Which are Dr.oh Patch UNII Codes?
The UNII codes for the active ingredients in this product are:
- CAMPHOR (NATURAL) (UNII: N20HL7Q941)
- CAMPHOR (NATURAL) (UNII: N20HL7Q941) (Active Moiety)
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Dr.oh Patch 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:
- EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6)
- THYMOL (UNII: 3J50XA376E)
- CASTOR OIL (UNII: D5340Y2I9G)
- .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
- GERANIOL (UNII: L837108USY)
- CITRONELLAL (UNII: QB99VZZ7GZ)
- CITRONELLA OIL (UNII: QYO8Q067D0)
- BENZOPHENONE (UNII: 701M4TTV9O)
- BENZYL BENZOATE (UNII: N863NB338G)
- ETHYL ACETATE (UNII: 76845O8NMZ)
What is the NDC to RxNorm Crosswalk for Dr.oh Patch?
- RxCUI: 1117074 - camphor 1.42 % / menthol 0.8 % Medicated Patch
- RxCUI: 1117074 - camphor 0.0142 MG/MG / menthol 0.008 MG/MG Medicated Patch
- RxCUI: 1117078 - Dr. Oh 1.42 % / 0.8 % Medicated Patch
- RxCUI: 1117078 - camphor 0.0142 MG/MG / menthol 0.008 MG/MG Medicated Patch [Dr. Oh Patch]
- RxCUI: 1117078 - Dr. Oh (camphor 1.42 % / menthol 0.8 % ) Medicated Patch
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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".