1 reports of this reaction
12.5% of all ZINC OXIDE SUNSCREEN reports
#2 most reported adverse reaction
DRY SKIN is the #2 most commonly reported adverse reaction for ZINC OXIDE SUNSCREEN, manufactured by Bausch Health US, LLC. There are 1 FDA adverse event reports linking ZINC OXIDE SUNSCREEN to DRY SKIN. This represents approximately 12.5% of all 8 adverse event reports for this drug.
Patients taking ZINC OXIDE SUNSCREEN who experience dry skin should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
DRY SKIN is a frequently reported adverse event for ZINC OXIDE SUNSCREEN, accounting for a significant proportion of all reports.
In addition to dry skin, the following adverse reactions have been reported for ZINC OXIDE SUNSCREEN:
The following drugs have also been linked to dry skin in FDA adverse event reports:
DRY SKIN has been reported as an adverse event in 1 FDA reports for ZINC OXIDE SUNSCREEN. This does not prove causation, but indicates an association observed in post-market surveillance data.
DRY SKIN accounts for approximately 12.5% of all adverse event reports for ZINC OXIDE SUNSCREEN, making it one of the most commonly reported side effect.
If you experience dry skin while taking ZINC OXIDE SUNSCREEN, contact your healthcare provider. They can evaluate whether the symptom is related to your medication and discuss potential adjustments to your treatment plan. Do not stop taking prescribed medication without consulting your doctor.