Sanitizetek
FDA Label NDC 81737-002

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Sanitizetek, Llc for the product Sanitizetek (NDC 81737-002). 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 other, otc - active ingredient, otc - purpose, indications & usage, warnings, otc - keep out of reach of children, dosage & administration, other safety information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

→ Other

→ Otc - Active Ingredient

→ Otc - Purpose

→ Indications & Usage

→ Warnings

→ Otc - Keep Out Of Reach Of Children

→ Dosage & Administration

→ Other Safety Information

→ Inactive Ingredient

→ Package Label

Other

Drug Facts

Otc - Active Ingredient

Active Ingredient
Isopropyl Alcohol, 75%

Otc - Purpose

Purpose
Antiseptic

Indications & Usage

Uses
♦ Hand sanitizer to help reduce bacteria on the skin that could cause disease
♦ Recommended for repeated use

Warnings

Warnings: Flammable. Keep away from fire or flame.
For external use only
When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash appears and persists

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.

Dosage & Administration

Directions

♦ Place enough product in your palm to thoroughly cover hands.
♦ Rub hands together briskly until dry.
♦ Children under 6 years of age should be supervised when using this product.