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Manufactured by Raining Rose, Inc
12 FDA adverse event reports analyzed
Last updated: 2026-04-15
HAND SANITIZER is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by Raining Rose, Inc. The most commonly reported adverse reactions for HAND SANITIZER include ALLERGY TO CHEMICALS, APPLICATION SITE DRYNESS, APPLICATION SITE RASH, BURNING SENSATION, ORAL DISCOMFORT. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for HAND SANITIZER.
Out of 5 classified reports for HAND SANITIZER:
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 12 FDA FAERS reports that mention HAND SANITIZER. Reporting is voluntary and does not prove that the drug caused any listed event.
Frequently reported terms in FAERS include ALLERGY TO CHEMICALS, APPLICATION SITE DRYNESS, APPLICATION SITE RASH, BURNING SENSATION, ORAL DISCOMFORT, PRODUCT ODOUR ABNORMAL. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.
Labeling and FAERS entries often list Raining Rose, Inc in connection with HAND SANITIZER. Always verify the specific product and NDC with your pharmacist.