NDC 71471-561 - Aqua Plus Acne Treatment System
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 71471-561
- Package NDCs from labels
- 71471-561-27
- Manufacturer
- Totally Clear Products, Inc
- Effective date
- 2017-12-23
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Aqua Plus Acne Treatment System - Totally Clear Products, Inc | Totally Clear Products, Inc | 2017-12-23 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 71471-561-27 | Aqua Plus Acne Treatment System | 50 mL in 1 BOTTLE | SOLUTION | 50 mL | 20 mg in 1mL | 3 |
DailyMed Dashboard NDC Coverage#
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.
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.