Exfo Tonic Acne Treatment Solution
FDA Label NDC 70764-104

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 Exfo Tonic Acne Treatment (NDC 70764-104). 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, questions or comments, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredients

SALICYLIC ACID (2.0%)

Purpose

ACNE TREATMENT

Use

AN ANTISEPTIC AND EXFOLIATING TONIC DESIGNED TO CONTROL EXCESSIVE OILINESS, REDUCE BREAKOUTS AND DISOLVE DEAD CELL BUILD UP.

Warnings

MAY TINGLE WHEN FIRST APPLIED. FOR EXTERNAL USE ONLY. WHEN USING THIS PRODUCT, AVOID CONTACT WITH EYES. IF CONTACT OCCURS, RINSE THOROUGHLY WITH WATER. AVOID UNNECESSARY SUN EXPOSURE AS THIS PRODUCT MAY INCREASE YOUR SENSITIVITY TO THE SUN. DISCONTINUE USE AND ASK A DOCTOR IF IRRITATION OR RASH DEVELOPS.

Directions

APPLY OR SPRAY ONTO TISSUE OR COTTON PAD, THEN APPLY TO ENTIRE FACE OR JUST THE ACNE-PRONE AREAS AS NEEDED. MAY BE APPLIED ONCE OR TWICE DAILY.

Inactive Ingredients

WATER, GLYCOLIC ACID (3%), SD ALCOHOL 40-A, HAMAMELIS VIRGINIANA (WITCH HAZEL) EXTRACT, PEG-40 HYDROGENATED CASTOR OIL.

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.

Questions Or Comments

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