Overnight Clearing
Overnight Clearing is an FDA drug label for the active ingredient SALICYLIC ACID manufactured by Dermalogica, Inc. administered by TOPICAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20171204.
Generic: SALICYLIC ACID
Manufacturer: Dermalogica, Inc.
Product Type: HUMAN OTC DRUG
Route: TOPICAL
Dosage Form:
NDC: 68479-706
Application: part358H
Effective: 20171204
Active Ingredients: Active Ingredients Salicylic Acid 2.0%
Indications & Usage
Indications For the treatment of acne.
Dosage & Administration
Directions Clean the skin thoroughly before applying. Cover the affected area with a thin layer at night. Because too much drying of the skin may occur, start with 1 application daily at night, and if bothersome dryness or peeling occurs, reduce application to 2 to 3 times per week.
Contraindications
Not available.
Warnings
Warnings For external use only. Do not use on broken skin or on large areas of the body. When using this product Apply to affected areas only Skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time. Avoid unnecessary sun exposure and use a sunscreen. Do not use in or near eyes. Stop use and ask a Doctor if rash occurs. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Adverse Reactions
Not available.
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