OTC - ACTIVE INGREDIENT SECTION
Active Ingredient:
Hydroquinone 2%
Active Ingredient:
Hydroquinone 2%
Purpose:
Skin Lightening Gel
Uses:
For gradual fading of dark (brownish) spots
Warnings:
Avoid contact with eyes. Children under 12 years of age; Do not use unless directed by a doctor.
Some users may experience a mild irritation. If skin irritation becomes severe, stop use and consult a doctor.
Directions:
Apply a small amount as a thin layer on the affected area or use as directed by a doctor. Sun exposure should be limited by using a sunscreen agent or a sun blocking agent.
Other Ingredients:
Water, Propylene Glycol, Carbomer, Sodium Palmitoyl Proline, Nymphaea Alba Flower Extract, glycerin, Citrus Unshiu Peel Extract, Sodium Hydroxymethylglycinate,Sodium Sulfite, Sodium Metabisulfite, Butylene Glycol, Phenoxyethanol, Disodium EDTA, Polysorbate 20, Trisodium EDTA, Benzophenone-4, EDTA, Caprylyl Glycol, Hexylene Glycol, Sodium Hydroxide, Caramel, Mica, Iron Oxides (CI 77491)
| Class | Version | Type | Effective |
|---|---|---|---|
| HYDROQUINONE Pharmacologic Class Indexing | 2 | Indexing - Pharmacologic Class | 20180813 |
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 85490a6b-2306-6bf2-c51b-eb63537dc2da | Product name | 1 | 20140508 |
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 59735-310-28 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-e0f8-f424-e053-dadaa90a57ce | Advanced Dual Complex Fade Gel Maximum Strength Plus |
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 59735-310-28 | Advanced Dual Complex FadeMaximum Strength Plus | 28.4 g in 1 BOTTLE, PUMP | GEL | 28.4 | 3 | |
| 59735-310-28 | Advanced Dual Complex FadeMaximum Strength Plus | 1 in 1 CARTON | GEL | 1 | 3 |
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| Hydroquinone | ACTIVE INGREDIENT | XV74C1N1AE | 3 | |
| Hydroquinone | ACTIVE MOIETY | XV74C1N1AE | 3 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 59735-310 | 59735-310-28 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| Hydroquinone | XV74C1N1AE | ACTIB |
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 |
|---|---|---|---|---|---|---|
| fed097e8-f13e-411b-b54c-5a7b0f433c84 | 6890a8c7-5561-4a39-bb77-f72ba7692879 | 2009-02-25 | Warnings | fed097e8-f13e-411b-b54c-5a7b0f433c84 6890a8c7-5561-4a39-bb77-f72ba7692879 |
Adverse event summaries are temporarily unavailable. Other product information remains available.