Ouhi Cell Power No 1 Essence
FDA Label NDC 53208-491

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 Ouhi Cell Power No 1 Essence (NDC 53208-491). 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, dosage & administration, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Otc - Active Ingredient

NIACINAMIDE 2%

HYDROXYPROLINE 0.5%

Otc - Purpose

Wrinkle/Whitening functional cosmetic.

Warnings

Stop use if rash or irritation develops and lasts.

Otc - When Using

Keep out of eyes. Rinse with water to remove.

Indications & Usage

Apply in the morning and evening after facial cleansing. Pump 1~2 times on your hand. Absorb in the essence by gently smoothing over your face with your fingertips along your face texture.

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, ALCOHOL, GLYCERETH-26, GLYCERIN, FRUIT, BIOSACCHARIDE GUM-1, METHYL GLUCETH-20, FILIPENDULA ULMARIA ROOT, YEAST, CETOSTEARYL ALCOHOL, TROMETHAMINE, EDETATE TRISODIUM, GERANIUM MACULATUM ROOT, PAEONIA LACTIFLORA ROOT, POLYDATIN.

Dosage & Administration

Use before the Skin or Toner.

Package Label.Principal Display Panel

OHUI

 CELL POWER NO.1

 ESSENCE


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