NDC 69842-856 Bite And Sting Medicated Relief Pads Cvs
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69842 - Cvs
- 69842-856 - Bite And Sting Medicated Relief Pads
Product Packages
NDC Code 69842-856-03
Package Description: 72 g in 1 JAR
Product Details
What is NDC 69842-856?
What are the uses for Bite And Sting Medicated Relief Pads Cvs?
Which are Bite And Sting Medicated Relief Pads Cvs UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZOCAINE (UNII: U3RSY48JW5)
- BENZOCAINE (UNII: U3RSY48JW5) (Active Moiety)
Which are Bite And Sting Medicated Relief Pads Cvs 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:
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
- CHAMOMILE (UNII: FGL3685T2X)
- CHOLECALCIFEROL (UNII: 1C6V77QF41)
- DIISOPROPYL ADIPATE (UNII: P7E6YFV72X)
- CLOVE OIL (UNII: 578389D6D0)
- PEPPERMINT OIL (UNII: AV092KU4JH)
- OCTYLDODECANOL (UNII: 461N1O614Y)
- OLIVE OIL (UNII: 6UYK2W1W1E)
- PEG-8 DIMETHICONE (UNII: GIA7T764OD)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- ALCOHOL (UNII: 3K9958V90M)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SODIUM PROPOXYHYDROXYPROPYL THIOSULFATE SILICA (UNII: 208G222332)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- CORN OIL (UNII: 8470G57WFM)
What is the NDC to RxNorm Crosswalk for Bite And Sting Medicated Relief Pads Cvs?
- RxCUI: 1927647 - benzocaine 5 % Medicated Pad
- RxCUI: 1927647 - benzocaine 50 MG/ML Medicated Pad
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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".