NDC 84483-0010-01 - LANOZEM HEMORRHOIDAL
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
- 84483-0010
- Requested NDC
- 84483-0010-01
- Package NDCs from labels
- 84483-0010-1, 84483-0010-01
- Manufacturer
- Sod-e Biotech Ltd
- Effective date
- 2025-05-07
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| LANOZEM HEMORRHOIDAL - Sod-e Biotech Ltd | Sod-e Biotech Ltd | 2025-05-07 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 84483-0010-1 | LANOZEM HEMORRHOIDAL | 3 g in 1 TUBE | OINTMENT | 3 | 1 | |
| 84483-0010-1 | LANOZEM HEMORRHOIDAL | 10 in 1 CARTON | OINTMENT | 10 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 84483-0010 | LANOZEM HEMORRHOIDAL (MENTHOL, PETROLATUM) OINTMENT [SOD-E BIOTECH LTD] | 1 | Current NDC, 2 package rows | 20250509_34901e83-8f24-8460-e063-6394a90a2744.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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Eagle Brand Medicated Oil Aromatic | CAMPHOR, MENTHOL, METHYL SALICYLATE | Borden Company (Private) Limited | 54e45d89-e8c3-6fc3-e063-6394a90aac4e | 2015-06-15 | Warnings | L7T10EIP3A |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.