NDC 42851-088 - ZO Skin Health Post Procedure Recovery 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
- 42851-088
- Package NDCs from labels
- 42851-088-06
- Manufacturer
- ZO Skin Health, Inc. | Bentley Laboratories, LLC
- Effective date
- 2024-12-27
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Aluminum Acetate - ZO Skin Health, Inc. | Bentley Laboratories, LLC | ZO Skin Health, Inc. | Bentley Laboratories, LLC | 2024-12-27 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 42851-088-06 | ZO Skin Health Post Procedure Recovery System | 6 g in 1 PACKET | POWDER | 6 g | 4866 mg in 6g | 5 |
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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.