Antibacterial
FDA Label NDC 63691-002

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Sun Products Corporation for the product Antibacterial (NDC 63691-002). 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 otc - active ingredient, indications & usage, warnings, otc - keep out of reach of children, otc - purpose, otc - questions, dosage & administration, inactive ingredient, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

→ Otc - Active Ingredient

→ Indications & Usage

→ Warnings

→ Otc - Keep Out Of Reach Of Children

→ Otc - Purpose

→ Otc - Questions

→ Dosage & Administration

→ Inactive Ingredient

→ Package Label.principal Display Panel

Otc - Active Ingredient

Drug Facts

Active ingredient

Triclosan 0.10% (or % in formula)

Indications & Usage

Use helps fight germs on hands when used as a hand soap

Warnings

For external use only

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. In case of eye contact, rinse thoroughly with water.