NDC 79481-0195-01 - Gentle Laxative
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
- 79481-0195
- Requested NDC
- 79481-0195-01
- Package NDCs from labels
- 79481-0195-1, 79481-0195-01
- Manufacturer
- MEIJER, INC. | GCP Laboratories
- Effective date
- 2024-05-22
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Gentle Laxative - MEIJER, INC. | GCP Laboratories | MEIJER, INC. | GCP Laboratories | 2024-05-22 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 79481-0195-1 | Gentle Laxative | 355 mL in 1 BOTTLE | LIQUID | 355 | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 79481-0195 | GENTLE LAXATIVE (MAGNESIUM HYDROXIDE) LIQUID [MEIJER, INC.] | 2 | Current NDC, 1 package rows | 20240524_11fe5bd0-585a-ad8a-e063-6294a90a3ae8.zip |
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.