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Benzocaine; Isopropyl Alcohol

Popular Brands: : Alcohol Prep Pads, Alcohol Swabs With Benzocaine, Alcohol Prep Swab With Pain Relief, Alcohol Swab With Benzocaine, Benzocaine; Isopropyl Alcohol
Official FDA Reports204
Social Media Events0
Total Posts0
Avg. Review Score0.00/ 5
Active Ingredients
  • Benzocaine; Isopropyl Alcohol
Approved Uses *
  • No other uses available

* Extracted from Drug Label

  • Amerisource Bergen
  • Cardinal Health
  • Changzhou Maokang Medical Products Co., Ltd
  • Dukal Corporation
  • H And P Industries, Inc. Dba Triad Group
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  This report is for all products sharing this active ingredient. For more details, please use our Workbench for research on individual brands like Alcohol Prep Pads.

* Extracted from FDA Adverse Event Report


The quarterly trend chart illustrates changing levels of adverse events over time. Results from both the FDA Adverse Event Database (FAERS) and adverse events extracted from social media by Druginformer are plotted side-by-side for easy comparison.

The proportion of people completing user reviews who complained about a side effect.

The proportion of social media adverse event complaints for each adverse event type.

The proportion of FAERS (FDA) adverse event complaints for each adverse event type.

Benzocaine; Isopropyl Alcohol Side Effects

  Social Media
(Online Comments)
(Reports Submitted to FDA)
Side Effect On Drug
Reports % of
Alarm Reports % of

* DrugInformer calculates alarm using a proprietary algorithm. Alarm should not be taken as an ofiicial signal from the FDA or other regulatory entity.

User Voices

The following are comments from users that experienced side effects while taking Benzocaine; Isopropyl Alcohol

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Additional Drug Information

* Warning: The facts and figures contained in these reports are accurate to the best of our capability; however, our metrics are only meant to augment your medical knowledge, and should never be used as the sole basis for selecting a new medication. As with any medical decision, be sure to work with your doctor to ensure the best choices are made for your condition.

* About FAERS: The FDA Adverse Event Reporting System (FAERS) is used by FDA for activities such as looking for new safety concerns that might be related to a marketed product, evaluating a manufacturer's compliance to reporting regulations and responding to outside requests for information. Reporting of adverse events is a voluntary process, and not every report is sent to FDA and entered into FAERS. The FAERS database may contain duplicate reports, the report quality is variable, and many factors may influence reporting (e.g., media attention, length of time a drug is marketed, market share). For these reasons, FAERS case reports cannot be used to calculate incidence or estimates of risk for a particular product or compare risks between products.