Topiclear Skin Lightening
FDA Label NDC 66129-040

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 Beauty Exchange for the product Topiclear Skin Lightening (NDC 66129-040). 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, warnings, otc - do not use, otc - when using, otc - purpose, indications & usage, dosage & administration, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Otc - Active Ingredient

Hydroquinone 2%

Warnings

For external use only

Otc - Do Not Use

On children under 12 years of age unless directed by a doctor

Otc - When Using

Avoid contact with eyes.

Otc - Purpose

Skin Lightener

Indications & Usage

For the gradual fading of dark (brownish) areas in the skin such as freckles, age and liver spots

Dosage & Administration

Apply a small amount as a thin layer on the affected area twice daily, or use as directed by a doctor

Otc - Keep Out Of Reach Of Children

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

Inactive Ingredient

WATER, CETOSTEARYL ALCOHOL, GLYCERIN, TROLAMINE, CARBOMER COPOLYMER TYPE A, SODIUM METABISULFITE, EDETATE DISODIUM

Package Label.Principal Display Panel

Image Of Product (Topi004)

Image Of Product (Topi004)

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