Hand Sanitizer
FDA Label NDC 49035-219

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Wal-mart Stores Inc. for the product Hand Sanitizer (NDC 49035-219). 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 otc - active ingredient, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Otc - Active Ingredient

​Drug Facts

​Active Ingredient

Ethyl Alcohol 63%

Purpose

Anticeptic

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