Antibacterial Foaming
FDA Label NDC 41520-169

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by American Sales Company for the product Antibacterial Foaming (NDC 41520-169). 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 using this product and ask doctor if, keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Triclosan 0.46%


Purpose

Antibacterial

Uses

For hand washing to decrease bacteria on the skin.

Warnings

For external use only.

When Using This Product

Avoid contact with eyes.  If contact occurs, rinse eyes thoroughly with water.

Stop Using This Product And Ask Doctor If

Irritation and redness develop.

Keep Out Of Reach Of Children

In case of accidental ingestion, get medical help and contact Poison Control Center immediately.

Directions

Pump onto dry hands, work into a lather and rinse thoroughly.

Other Information

Store at room temperature.

Inactive Ingredients

WATER, SODIUM XYLENE SULFONATE, DIPROPYLENE GLYCOL, GLYCERIN, SODIUM PCA, AMMONIUM LAURYL SULFATE, COCAMIDOPROPYL BETAINE, POLYQUATERNIUM-10, FRAGRANCE, DISODIUM PHOSPHATE, CETYL ALCOHOL, ALOE BARBADENSIS LEAF JUICE, CITRIC ACID, METHYLPARABEN, PROPYLPARABEN, RED 4 (CI 14700), YELLOW 5 (CI 19140).

Package Label.Principal Display Panel

Image Of Antibacterial Foaming (C3)

Image Of Antibacterial Foaming (C3)

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