NDC 59779-613 Cvs Medicated Chest Rub Roll-on
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 59779-613?
What are the uses for Cvs Medicated Chest Rub Roll-on?
Which are Cvs Medicated Chest Rub Roll-on UNII Codes?
The UNII codes for the active ingredients in this product are:
- CAMPHOR (NATURAL) (UNII: N20HL7Q941)
- CAMPHOR (NATURAL) (UNII: N20HL7Q941) (Active Moiety)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- EUCALYPTUS OIL (UNII: 2R04ONI662) (Active Moiety)
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Cvs Medicated Chest Rub Roll-on 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:
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
- ALCOHOL (UNII: 3K9958V90M)
- ALLANTOIN (UNII: 344S277G0Z)
- AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
- LEVOMENOL (UNII: 24WE03BX2T)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- THYME OIL (UNII: 2UK410MY6B)
- WATER (UNII: 059QF0KO0R)
- XANTHAN GUM (UNII: TTV12P4NEE)
What is the NDC to RxNorm Crosswalk for Cvs Medicated Chest Rub Roll-on?
- RxCUI: 1547992 - camphor 4.8 % / eucalyptus oil 1.2 % / menthol 2.6 % Topical Gel
- RxCUI: 1547992 - camphor 0.048 MG/MG / Eucalyptus oil 0.012 MG/MG / menthol 0.026 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".