Smith And Johnson Antibacterial
FDA Label NDC 52546-100

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Allied International Corp for the product Smith And Johnson Antibacterial (NDC 52546-100). 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, uses, warnings, directions, inactive ingredient, description, keep out of reach of children., purpose:, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Warnings

Warnings

For external use only.

When using this product avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.

Keep out of reach of children.

If swallowed, contact a poison control center immediately and consult a physician if necessary.

Inactive Ingredient

Inactive Ingredients

Water, Sodium Laureth Sulfate, Cocamidopropyl Betaine, Cocamide DEA, Sodium Chloride, Citric Acid, Fragrance, DMDM Hydantoin, Tetrasodium EDTA

Description

Designed in USA

Made in China for

Allied International Corp of VA

PO Box 858 Ashburn, VA 20146 USA

www.alliedint.com

Package Label.Principal Display Panel

Smith and Johnson

New

Liquid Soap

Antibacterial

16 FL OZ (470 ML)

Liquidsoap (Liquidsoap)

Liquidsoap (Liquidsoap)

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