Eradikate Daily Foaming Cleanser Acne Treatment
- Product NDC
- 56152-0268
- 11-digit product format
- 561520268
- Labeler code
- 56152
- Product ID
- 56152-0268_5b78972c-793a-d406-e063-6294a90afb00
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sulfur
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Cosmetic Enterprises Ltd
- Application
- M006
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-08-25
- Substance
- SULFUR
- Active strength
- 3 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Eradikate Daily Foaming Cleanser Acne Treatment
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| SULFUR | 3 g/100mL |
openFDA label cross-check#
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.
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 56152-0268-2 | 56152026802 | 1 TUBE in 1 CARTON (56152-0268-2) / 30 mL in 1 TUBE (56152-0268-1) | 1 tube | 2026-08-25 | No | No | Current |
| 56152-0268-4 | 56152026804 | 1 TUBE in 1 CARTON (56152-0268-4) / 120 mL in 1 TUBE (56152-0268-3) | 1 tube | 2026-08-25 | No | No | Current |