Label: EXFO TONIC ACNE TREATMENT- salicylic acid solution
- NDC Code(s): 70764-104-11, 70764-104-51
- Packager: CONTROL CORRECTIVE SKINCARE INC
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated September 22, 2023
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- ACTIVE INGREDIENTS
- PURPOSE
- USE
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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
- INACTIVE INGREDIENTS
- KEEP OUT OF REACH OF CHILDREN
- QUESTIONS OR COMMENTS
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
EXFO TONIC ACNE TREATMENT
salicylic acid solutionProduct 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)