Otc - Active Ingredient
Salicylic Acid
Dr.zium All Clear Spot
FDA Label NDC 69278-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Gm Holdings Co., Ltd for the product Dr.zium All Clear Spot (NDC 69278-001). 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 otc - active ingredient, inactive ingredient, otc - purpose, indications & usage, warnings, dosage & administration, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Inactive Ingredient
Niacinamide, Terminalia Ferdinandiana Fruit Extract, Aazelaoyl Octapeptide-9, Water, etc
Otc - Purpose
Acne Treatment
Indications & Usage
Apply an adequate amount to the trouble area and absorb with gentle dabbing
Warnings
Warnings
Do not use if you have very sensitive skin or are sensitive to Salicylic Acid
Ask a doctor or pharmacist before use if you are using other topical acne medications at the same time or immediately following use of this product. This may increase dryness or irritation of the skin. If this occurs, only one medication should be used unless directed by a doctor.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Dosage & Administration
For external use only
Package Label.Principal Display Panel
Label (Label)
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