NDC 86152-0071-2 - F10
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
- 86152-0071
- Requested NDC
- 86152-0071-2
- Package NDCs from labels
- 86152-0071-2
- Manufacturer
- Health and Hygiene (Pty) Ltd | Lonza Group AG
- Effective date
- 2022-01-28
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| F10 - Health and Hygiene (Pty) Ltd | Lonza Group AG | Health and Hygiene (Pty) Ltd | Lonza Group AG | 2022-01-28 | PRESCRIPTION ANIMAL DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 86152-0071-2 | F10 | 200 mL in 1 BOTTLE, PLASTIC | LIQUID | 200 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 86152-0071 | F10 (F10 ANTISEPTIC SOLUTION CONCENTRATE) LIQUID [HEALTH AND HYGIENE (PTY) LTD] | 1 | 1 package rows | 20220129_631638e3-ce2c-4a16-b9fa-182e63e9ab89.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.