Active Ingredients
SALICYLIC ACID (2.0%)
Acne Spot Treatment Gel
FDA Label NDC 70764-105
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Control Corrective Skincare Inc for the product Acne Spot Treatment (NDC 70764-105). 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 ingredients, purpose, use, warnings, directions, inactive ingredients, otc - keep out of reach of children, otc - do not use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
ACNE TREATMENT
Use
AN EXFOLIATING GEL THAT AIDS IN REDUCING ACNE BREAKOUTS.
Warnings
FOR EXTERNAL USE ONLY. DO NOT USE ON BROKEN SKIN. AVOID CONTACT WITH EYES. IF CONTACT OCCURS, RINSE THOROUGHLY WITH WATER.
Directions
APPLY A SMALL AMOUNT WITH FINGERS TO CLEAN, DRY SKIN. MAY BE USED ALL OVER THE AFFECTED AREA OR USED TO SPOT TREAT BLEMISHES. IF ANY DISCOMFORT OCCURS, REDUCE FREQUENCY OR DISCONTINUE USE.
Inactive Ingredients
WATER, GLYCOLIC ACID (3%), SD ALCOHOL 40-A, ALOE BARBADENSIS LEAF JUICE, WITCH HAZEL, GLYCERIN, TRIETHANOLAMINE, METHYL GLUCETH-20, SODIUM LACTATE, FRUCTOSE, UREA, NIACINAMIDE, INOSITOL, SODIUM BENZOATE, LACTIC ACID, HYDROXYETHYLCELLULOSE, PHENOXYETHANOL, PANTHENOL, ALLANTOIN, GLUCOSAMINE SULFATE, METHYLISOTHIAZOLINONE.
Otc - Keep Out Of Reach Of Children
KEEP OUT OF REACH OF CHILDREN. IF SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.
Otc - Do Not Use
DO NOT USE IF ALLERGIC TO ASPERIN.
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