NDC 69842-731 Bite And Sting Relief Stick
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69842 - Cvs Health
- 69842-731 - Bite And Sting Relief Stick
Product Packages
NDC Code 69842-731-01
Package Description: 1 TUBE, WITH APPLICATOR in 1 CARTON / 14.79 g in 1 TUBE, WITH APPLICATOR
Product Details
What is NDC 69842-731?
What are the uses for Bite And Sting Relief Stick?
Which are Bite And Sting Relief Stick UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZOCAINE (UNII: U3RSY48JW5)
- BENZOCAINE (UNII: U3RSY48JW5) (Active Moiety)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (Active Moiety)
- PHENOL (UNII: 339NCG44TV)
- PHENOL (UNII: 339NCG44TV) (Active Moiety)
Which are Bite And Sting Relief Stick 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:
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
What is the NDC to RxNorm Crosswalk for Bite And Sting Relief Stick?
- RxCUI: 1435257 - benzocaine 5 % / camphor 3 % / phenol 1.35 % Topical Solution
- RxCUI: 1435257 - benzocaine 50 MG/ML / camphor 30 MG/ML / phenol 13.5 MG/ML Topical Solution
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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".