Ferino Hand Sanitizer
FDA Label NDC 80359-002

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Ferino Distillery for the product Ferino Hand Sanitizer (NDC 80359-002). 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 drug facts, active ingredient, purpose, uses, directions, other info, inactive ingredients, for more info, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Drug Facts

Active Ingredient

Ethyl Alcohol 70%

Purpose

Antiseptic

Uses

Hand sanitizer to help reduce bacteria on the skin that can cause disease.

Directions

Apply liberally to front and back of hands. Allow to dry. Recommended for repeat use.

Other Info

Store between 0° C (32° F) - 41° C (105° F)

Inactive Ingredients

Methylcellulose, Water, Fragrance

For More Info

Ferinodistillery.com

775.433.2033

Warnings

For external use only: hands.

Flammable, keep away from fire or flame.

When using this product avoid contact with eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask doctor if irritation or redness appears and lasts.

Otc - Keep Out Of Reach Of Children

If swallowed get medical help or contact a Poison Control Center immediately.

Do not use: in children less than 2 months of age and open wounds. Do not inhale or ingest. Supervise children under 6 years of age when using this product to avoid swallowing.

Packaging

Image (8035900211lb)

Image (8035900211lb)

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