Steiro
FDA Label NDC 76079-001

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Bioblockade Llc for the product Steiro (NDC 76079-001). 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, inactive ingredients, purpose, uses, directions, keep out of reach of children, warning, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Active Ingredient

Benzalkonium Chloride 0.13%

Inactive Ingredients

Water, Tocopheryl Acetate, Polysorbate 20, Polyaminopropyl Biguanide, Phenooxythanol, Methylparaben, Ethylparaben, Propylparaben, Butylparaben, and Isobutylparaben

Purpose

Antimicrobial

Uses

For Sanitizing to decrease bacteria on the skin,  safe for repeated use

Directions

Place a small amount on skin and rub until dry. 

Keep Out Of Reach Of Children

Children under 6 years of age should be supervised when using this product.

Warning

For external use only.  When using this product avoid contact with the eyes.  If in eyes flush with water.  Do not ingest.   Discontinue use and contact a doctor if irritation and redness develop and if conditions persist for more than 72 hours.

Other Information

Do not store above 110 degrees F (43 C)  store in an area inaccessible to children.

Package Label

Steiro Lotion  Kills Germs  A Total Hand / Skin Sanitizer  Foam Hand / Skin Sanitizer Alcohol and Fragrance Free  Moisturizing and conditioning formula  Net Contents: 210 ml/7.1 fl.oz.

Manufactured for Bioblockade LLC  Houma, LA 70364

Steiro Lotion Label (Steiro Lotion Label)

Steiro Lotion Label (Steiro Lotion Label)

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