Bak Liquid
FDA Label NDC 12745-145

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Medical Chemical Corporation for the product Bak (NDC 12745-145). 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 - purpose, otc - active ingredient, otc - keep out of reach of children, indications & usage, warnings, dosage & administration, inactive ingredient, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Otc - Purpose

Antiseptic

Otc - Active Ingredient

Active Ingredient: Alkyl (50% C14, 40% C12, 10% C10) dimethyl benzyl ammonium chloride, 1.33 g/l.  Assayed by a non-USP method.

Otc - Keep Out Of Reach Of Children

Warnings:  Keep out of reach of children.  Mixing this solution with soaps or detergents will destroy its germicidal properties.

Indications & Usage

Uses: Intended for use as a general purpose topical antiseptic for first-aid treatment of minor cuts and abrasions.

Warnings

Caution:  Mixing this solution with soaps or detergents will destroy its germicidal properties.

Dosage & Administration

Usage: Apply to affected area for first-aid treatment of minor cuts and abrasions.  Discontinue use and get medical aid if redness, irritation or infection develops.  In case of deep or puncture wounds consult a physician.

Inactive Ingredient

Inactive Ingredients: Water

Package Label.Principal Display Panel

baklabel.jpg

Bak Label (Baklabel)

Bak Label (Baklabel)

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