Hand Sanitizer
FDA Label NDC 76810-101
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Hand Sanitizer Company Llc for the product Hand Sanitizer (NDC 76810-101). 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, warnings, otc - keep out of reach of children, 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
Antimicrobial
Warnings
For external use only: hands
Flammable, keep away from fire or flame
When using this product ■ keep out of eyes. In case of contact with eyes, flush thoroughly with water. ■ avoid contact with broken skin ■ do not inhale or ingest.
Stop use and ask a doctor if ■ irritation and redness develop ■ condition persists for more than 72 hours
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away
Packaging
Image (Label4)
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