O Hui White Extreme Cellight
FDA Label NDC 53208-507

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Lg Household And Healthcare, Inc. for the product O Hui White Extreme Cellight (NDC 53208-507). 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, otc - purpose, warnings, otc - when using, indications & usage, otc - keep out of reach of children, inactive ingredient, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Otc - Active Ingredient

PROTOCATECHUALDEHYDE 0.032%

Otc - Purpose

Whitening cream

Warnings

Stop use if rash or irritation develops and lasts.

Otc - When Using

Keep out of eyes. Rinse with water to remove.

Indications & Usage

Use to whiten skin.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. Is swallowed, get medical help or contact a Poison Control Center right away.

Inactive Ingredient

WATER, DIPROPYLENE GLYCOL, CYCLOPENTASILOXANE, GLYCERIN, MEDIUM-CHAIN TRIGLYCERIDES, NEOPENTYL GLYCOL DICAPRATE, TREHALOSE, SQUALANE, 1,2-HEXANEDIOL, GLYCERYL STEARATE, DIMETHICONE, PANTHENOL, ALCOHOL, PHENOXYETHANOL, COPPER, ALPHA-TOCOPHEROL, EDETATE TRISODIUM, TROLAMINE, SODIUM METABISULFITE.

Package Label.Principal Display Panel

OHUI

WHITE EXTREME

CELLIGHT CREAM

Dosage & Administration

Use as needed to whiten skin.

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