Instant Hand Sanitizer
FDA Label NDC 79134-005

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Perfect Medics, Inc for the product Instant Hand Sanitizer (NDC 79134-005). 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 active ingredient(s), purpose, use, warnings, do not use, otc - when using, otc - stop use, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

→ Active Ingredient(s)

→ Purpose

→ Use

→ Warnings

→ Do Not Use

→ Otc - When Using

→ Otc - Stop Use

→ Otc - Keep Out Of Reach Of Children

→ Directions

→ Other Information

→ Inactive Ingredients

→ Package Label - Principal Display Panel

Active Ingredient(S)

Alcohol 75% v/v. Purpose: Antiseptic

Purpose

Antiseptic

Use

to decrease bacteria on the skin that could cause disease;recommended for repeated use

Warnings

For external use only-hands. Flammable. Keep away from heat or flame

Do Not Use

in children less than 2 months of age
on open skin wounds

Otc - When Using

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 skin irritation develops.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.