Dawn Ultra Antibacterial Hand Soap
FDA Label NDC 37000-617

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by The Procter & Gamble Manufacturing Company for the product Dawn Ultra Antibacterial Hand (NDC 37000-617). 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 other, active ingredient, purpose, use, warnings, otc - keep out of reach of children, directions, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Other

Drug Facts

Distributed by PROCTER & GAMBLE,
CINCINNATI, OH 45202

Active Ingredient

Chloroxylenol 0.30%

Purpose

Antibacterial hand soap

Use

  • for handwashing to decrease bacteria on the skin

Warnings

For external use only

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. In case of accidental ingestion, drink a glass of water to dilute. If eye contact occurs, rinse thoroughly with water.

Directions

  • wet hands and forearms. Apply 5 ml or palmful to hands and forearms. Scrub thoroughly for 30 sec. and rinse.

Questions?

1-800-725-3296

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