OTC - ACTIVE INGREDIENT SECTION
Active ingredient Purpose
Salicylic Acid (0.5%)..........Acne Medication
Active ingredient Purpose
Salicylic Acid (0.5%)..........Acne Medication
Purpose
Acne Medication
Use for the management of acne
Warnings: For external use only. Using other topical acne medications at the same time or immediately following use of this product may increase dryness or irritation of the skin. If this occurs, only one medication should be used unless directed by a doctor. Sensitivity test for new users: Apply product sparingly to one or two small affected areas during the first three days. If no discomfort occurs, follow the steps stated in directions.
Keep out of reach of children. In case of accidental ingestion, get medical help or contact a Poison Control Center right away.
Directions: Cleanse the skin thoroughly before applying medication. Use the pad to wipe the entire affected area one to three times daily. . Repeat with a clean pad as necessary to remove remaining traces of dirt. . Because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor. .If bothersome dryness or peeling occurs, reduce application to once a day or every other day.
Other ingredients: Aqua, Sodium Methyl 2-Sulfolaurate, Disodium 2-Sulfolaurate, Sodium Xylene Sulfonate, Menthol, *CO Glycerin, *CO Humulus Lupulus (Hops) Extract, *CO Lavandula Angustifolia (Lavender) Flower/Leaf/Stem Extract, *CO Calendula Officinalis Flower Extract, *CO Chamomilla Recutita (Matricaria) Flower Extract, *CO Citrus Limon (Lemon) Peel Extract, *CO Cucumis Sativus (Cucumber) Seed Extract, *CO Camellia Sinensis Leaf Extract, *CO Pyrus Malus (Apple) Fruit Extract, *CO Spirulina Platensis Extract, Disodium EDTA, Simethicone, Ethylhexylglycerin, Phenoxyethanol, Fragrance.
*CO Certified Organic
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 68062-9004-1 | 2023-01-30 | C162847 | 48780-1 | f386c649-e5e1-0266-e053-dadaa90a7c1a | Acne Treatment Pads |
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 68062-9004-1 | Acne Treatment Pads | 50 mL in 1 TUBE | LOTION | 50 | 2 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 68062-9004 | 68062-9004-1 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| GLYCERIN | PDC6A3C0OX | IACT |
| MENTHOL | L7T10EIP3A | IACT |
| SALICYLIC ACID | O414PZ4LPZ | ACTIB |
| WATER | 059QF0KO0R | IACT |
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Acne Treatment Pads | SALICYLIC ACID | Spa de Soleil | cc0f8f77-1942-22be-e053-2a95a90a3d7f | 2026-04-30 | Warnings | 68062-9004-1 68062-9004 68062900401 50b6e826-3ec8-ee59-e063-6294a90a43eb cc0f8f77-1942-22be-e053-2a95a90a3d7f |
Adverse event summaries are temporarily unavailable. Other product information remains available.