Drp Hand Sanitizer
FDA Label NDC 79202-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Europremier, S.a. De C.v. for the product Drp Hand Sanitizer (NDC 79202-001). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding drug facts, active ingredients, purpose, packaging, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredients
Ethyl alcohol 70%
Purpose
Antiseptic Alcohol
Packaging
Image (Drpga001)
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