Solgreat Alcohol-free Hand Sanitizer
FDA Label NDC 73913-004

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Panatural Usa, Inc. for the product Solgreat Alcohol-free Hand Sanitizer (NDC 73913-004). 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 lngredient, purpose, uses, warnings, directions, inactive ingredients, keep out of reach of children, products label-237ml solgreat alcohol-free hand sanitizer, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Lngredient

Benzalkonium Chloride

Purpose

Antibacterial

Uses

  • hand sanitizer to help decrease bacteria on the skin, when water, soap & towel are not available.
  • recommended for repeated use

Warnings


For external use only.

Flammable. Keep away from fire or flame.

Do not apply around eyes. Do not use in ears & mouth.

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

Stop use and ask a doctor if redness or irritation develop and persist for more than 72 hours.

Directions

  • place enough product into your palms and thoroughly spread on both hands.
  • rub into skin until dry.

Inactive Ingredients

BUTYLENE GLYCOL, CITRIC ACID, DIAZOLIDINYL UREA, HYDROXYETHYCELLULOSE, PEG-40 HYDROGENATE CASTOR OIL, PROPYLENE GLYCOL, WATER.

Keep Out Of Reach Of Children

Children must be supervised in use of this product

* Please review the disclaimer below.