EXFO TONIC ACNE TREATMENT- salicylic acid solution

EXFO TONIC ACNE TREATMENT by

Drug Labeling and Warnings

EXFO TONIC ACNE TREATMENT by is a Otc medication manufactured, distributed, or labeled by CONTROL CORRECTIVE SKINCARE INC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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.

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

WWW.CONTROLCORRECTIVE.COM

TOLL FREE 1-866-290-4290  

MADE IN USA

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

EXFO TONIC ACNE TREATMENT 
salicylic acid solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70764-104
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	2 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCOLIC ACID (UNII: 0WT12SX38S)
ALCOHOL (UNII: 3K9958V90M)
WITCH HAZEL (UNII: 101I4J0U34)
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70764-104-51	1 in 1 BOX	06/09/2016
1	NDC: 70764-104-11	198 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333D	06/09/2016

Labeler - CONTROL CORRECTIVE SKINCARE INC (023999357)