Hand Sanitizer Forest Scent
FDA Label NDC 73861-001

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Great Eagle Group Inc for the product Hand Sanitizer Forest Scent (NDC 73861-001). 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 lngredient, purpose, uses, warnings, directions, inactives, product label, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Lngredient

ETHYL ALCOHOL

Purpose

Antiseptic 

Uses

Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Recomended for repeated use.

Warnings

  • For external use only
  • Flammable
  • Keep away from heat and flame.
  •  Do not use in ear , mouth OR eyes.
  • When using this product

    •   Avoid contact with eyes. In case of eye contact, flush with water.

    • Keep out of reachof children.

      • If swallowed, seek medical attention immidately.

Directions

Pump as needed in to your palms and throughly spread on both hand.

Rub into skin until dry.

Inactives

Deionized Water, 
D-Panthenol
Fragrance
o-Cymen-5-ol
Thymus Vulgaris (Thyme) Flower/Leaf Extract

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