Otc - Active Ingredient
Otc-active Ingredient Section (Label)
Numbing Cream
FDA Label NDC 85524-2605
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Flexigo Inc for the product Numbing (NDC 85524-2605). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding otc - active ingredient, otc - do not use, otc - when using, otc - keep out of reach of children, otc - purpose, dosage & administration, inactive ingredient, warnings, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Do Not Use
Otc-active Ingredient Section (Label)
Otc - When Using
Otc-active Ingredient Section (Label)
Otc - Keep Out Of Reach Of Children
Otc-active Ingredient Section (Label)
Otc - Purpose
Otc-active Ingredient Section (Label)
Dosage & Administration
Otc-active Ingredient Section (Label)
Inactive Ingredient
Otc-active Ingredient Section (Label)
Warnings
Otc-active Ingredient Section (Label)
Storage And Handling
Otc-active Ingredient Section (Label)
Indications & Usage
Otc-active Ingredient Section (Label)
Recent Major Changes
Otc-active Ingredient Section (Label)
Package Label.Principal Display Panel
Otc-active Ingredient Section (Label)
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