ADVERSE EVENT REPORT
The FDA considers hand sanitizer an over-the-counter drug. As such, we are required to collect and report any adverse effects encountered by our customers to the FDA by providing them with the information found in form below.
The FDA considers an Adverse Event to be any undesirable event that is associated with the use of a drug or biological product in humans whether or not considered product-related by the applicant. For example: rash, burn, skin peeling, skin cracking, redness, etc.
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