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Manufactured by Casad Company Inc.
27 FDA adverse event reports analyzed
Last updated: 2026-04-15
LIP BALM is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by Casad Company Inc.. The most commonly reported adverse reactions for LIP BALM include TREMOR, ACNE CONGLOBATA, ACNE PUSTULAR, APPLICATION SITE ERYTHEMA, APPLICATION SITE IRRITATION. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for LIP BALM.
Out of 9 classified reports for LIP BALM:
The FDA classifies an adverse event as “serious” if it results in death, hospitalization, disability, congenital anomaly, or requires intervention to prevent permanent damage.
Demographics reflect voluntary FDA adverse event reporting patterns and may not represent the full patient population.
This profile reflects 27 FDA FAERS reports that mention LIP BALM. Reporting is voluntary and does not prove that the drug caused any listed event.
Frequently reported terms in FAERS include TREMOR, ACNE CONGLOBATA, ACNE PUSTULAR, APPLICATION SITE ERYTHEMA, APPLICATION SITE IRRITATION, BALANCE DISORDER. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.
Labeling and FAERS entries often list Casad Company Inc. in connection with LIP BALM. Always verify the specific product and NDC with your pharmacist.