NDC 69842-418 Cvs Health Healing On The Go Kit
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 69842-418?
What are the uses for Cvs Health Healing On The Go Kit?
Which are Cvs Health Healing On The Go Kit UNII Codes?
The UNII codes for the active ingredients in this product are:
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- ISOPROPYL ALCOHOL (UNII: ND2M416302) (Active Moiety)
- BACITRACIN ZINC (UNII: 89Y4M234ES)
- BACITRACIN (UNII: 58H6RWO52I) (Active Moiety)
- POLYMYXIN B SULFATE (UNII: 19371312D4)
- POLYMYXIN B (UNII: J2VZ07J96K) (Active Moiety)
- NEOMYCIN SULFATE (UNII: 057Y626693)
- NEOMYCIN (UNII: I16QD7X297) (Active Moiety)
- BENZOCAINE (UNII: U3RSY48JW5)
- BENZOCAINE (UNII: U3RSY48JW5) (Active Moiety)
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Cvs Health Healing On The Go Kit 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)
- PETROLATUM (UNII: 4T6H12BN9U)
- MINERAL OIL (UNII: T5L8T28FGP)
What is the NDC to RxNorm Crosswalk for Cvs Health Healing On The Go Kit?
- RxCUI: 1046313 - benzocaine 6 % / ethanol 60 % Medicated Pad
- RxCUI: 1046313 - benzocaine 60 MG/ML / ethanol 0.6 ML/ML Medicated Pad
- RxCUI: 1046313 - benzocaine 6 % / ethanol 60 % Topical Swab
- RxCUI: 204602 - bacitracin 400 UNT / neomycin 3.5 MG / polymyxin B 5000 UNT per GM Topical Ointment
- RxCUI: 204602 - bacitracin 0.4 UNT/MG / neomycin 0.0035 MG/MG / polymyxin B 5 UNT/MG Topical Ointment
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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".