Movate Skin Lightening
FDA Label NDC 66129-140

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 Movate Skin Lightening (NDC 66129-140). 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 - purpose, otc - when using, otc - do not use, otc - keep out of reach of children, inactive ingredient, indications & usage, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Otc - Active Ingredient

Hydroquinone 2%

Ethylhexyl Methoxycinnamate (Octyl Methoxycinnamate) 0.5%

Warnings

For external use only

Otc - Purpose

Skin Lightener

Otc - When Using

Avoid contact with the eyes

Otc - Do Not Use

On children under 12 years of age unless 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


Indications & Usage


Dosage & Administration


Package Label.Principal Display Panel

Image Of Product (Mov001)

Image Of Product (Mov001)

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