NDC 59779-057 Cvs Chest Rub
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 59779 - Cvs Pharmacy
- 59779-057 - Cvs Chest Rub
Product Packages
NDC Code 59779-057-24
Package Description: 1 JAR in 1 CARTON / 100 g in 1 JAR
NDC Code 59779-057-57
Package Description: 1 JAR in 1 CARTON / 50 g in 1 JAR
Product Details
What is NDC 59779-057?
What are the uses for Cvs Chest Rub?
Which are Cvs Chest Rub UNII Codes?
The UNII codes for the active ingredients in this product are:
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (Active Moiety)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- EUCALYPTUS OIL (UNII: 2R04ONI662) (Active Moiety)
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Cvs Chest Rub 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:
- PETROLATUM (UNII: 4T6H12BN9U)
- JUNIPERUS VIRGINIANA TWIG (UNII: 532BCG080L)
- TURPENTINE (UNII: XJ6RUH0O4G)
- THYMOL (UNII: 3J50XA376E)
- NUTMEG OIL (UNII: Z1CLM48948)
What is the NDC to RxNorm Crosswalk for Cvs Chest Rub?
- RxCUI: 727137 - camphor 4.8 % / eucalyptus oil 1.2 % / menthol 2.6 % Topical Ointment
- RxCUI: 727137 - camphor 0.048 MG/MG / Eucalyptus oil 0.012 MG/MG / menthol 0.026 MG/MG Topical Ointment
- RxCUI: 727137 - camphor 4.8 % / eucalyptus oil 1.2 % / menthol 2.6 % Chest Rub
- RxCUI: 727137 - camphor 4.8 % / eucalyptus oil 1.2 % / menthol 2.6 % Topical Stick
* 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".