Antibacterial Golden Burst
FDA Label NDC 52862-120

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by International Wholesale, Inc. for the product Antibacterial Golden Burst (NDC 52862-120). 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, purpose, uses, warnings, when using this product:, stop use and ask a doctor if:, keeps out of reach of children., directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Active Ingredient

Triclocarban 0.30%

Purpose

Antibacterial

Uses

  • Helps reduce bacteria on the skin that could cause disease.
  • Recommended for repeated use

Warnings

For external use only

When Using This Product:

do not use in or near the eyes. In case of eye contact, rinse eyes thoroughly with water.

Stop Use And Ask A Doctor If:

irritation and redness develops and lasts more than 72 hours.

Keeps Out Of Reach Of Children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • Wet bar with water
  • Lather vigorously and wash skin
  • Rinse and dry thoroughly

Other Information

  • Store below 110° F (43° C)
  • May discolor certain fabrics or surfaces

Inactive Ingredients

Sodium Cocoate, Sodium Palmate, Water, Glycerin, Sodium Chloride, Titanium Dioxide, BHT, Fragrance, FD&C Yellow #5

Package Display

Label (Pic)

Label (Pic)

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