Resurface Mask
FDA Label NDC 71276-150

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Ulab for the product Resurface Mask (NDC 71276-150). 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 active ingredient, inactive ingredient, purpose, warnings, keep out of reach of children, indications & usage, dosage & administration, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Active Ingredient

Active ingredients: GLYCERIN 6.83%

Inactive Ingredient

Inactive ingredients: AQUA (WATER), LACTIC ACID, BUTYLENE GLYCOL, GLYCOLIC ACID, SODIUM HYDROXIDE, DEHYDROXANTHAN GUM, ORYZA SATIVA (RICE) POWDER, POLYETHYLENE, SODIUM BENZOATE, PHENOXYETHANOL, PPG-26-BUTETH-26, PEG-40 HYDROGENATED CASTOR OIL, PARFUM (FRAGRANCE), DISODIUM EDTA, PROPYLENE GLYCOL, BACILLUS FERMENT, POTASSIUM SORBATE

Purpose

Purpose: Skin exfoliating gel mask

Warnings

Warnings: For external use only Avoid contact with eyes and eye contour area Discontinue use if signs of irritation or rashes appear. In case of contact with eyes, rinse immediately.

Keep Out Of Reach Of Children

KEEP OUT OF REACH OF CHILDREN

Indications & Usage

Indications & Usage: Use up to twice a month for a soft peeling or once a month for a strong peeling

Dosage & Administration

Dosage & Administration: Leave on for 5 - 10 minutes then rub with water on fingertips before rinse with lukewarm water or soaked sponge

* Please review the disclaimer below.