Nurinse Hand Sanitizer
FDA Label NDC 77368-070

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Nugentec for the product Nurinse Hand Sanitizer (NDC 77368-070). 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 ingredients:, inactive ingredients:, directions:, warnings:, other information:, packaging, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

→ Active Ingredients:

→ Inactive Ingredients:

→ Directions:

→ Warnings:

→ Other Information:

→ Packaging

Active Ingredients:

Ethanol Alcohol 70% v/v,

Inactive Ingredients:

Glycerin (for moisturizing), Hydrogen Peroxide, Water

Directions:

When using NuRinse Hand Sanitizer, apply a palmful of the product to one hand and rub the product all over the surfaces of both hands until your hands are dry. Do not wipe away excess sanitizer. For children under 6, use only with adult supervision. Not recommended for infants.

Warnings:

Flammable: Keep away from heat and flame. Keep container closed when not in use.
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.