NDC 53997-002-01 - Lansinoh Anti-itch
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
- 53997-002
- Requested NDC
- 53997-002-01
- Package NDCs from labels
- 53997-002-01, 53997-002-02
- Manufacturer
- Lansinoh Laboratories Inc | Dhaliwal Pharmaceuticals Laboratories, LLC
- Effective date
- 2024-12-22
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Lansinoh Anti Itch | Lansinoh Laboratories Inc | Dhaliwal Pharmaceuticals Laboratories, LLC | 2024-12-22 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 53997-002-01 | Lansinoh Anti-itch | 125 mL in 1 TUBE | CREAM | 125 | 2 | |
| 53997-002-02 | Lansinoh Anti-itch | 1 in 1 CARTON | CREAM | 1 | 2 |
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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| DG 3x Medicated Toothache adn Gum Gel | BENZOCAINE | Dollar General | b2c0e442-4cba-589d-e053-2995a90a6bca | 2025-11-14 | Warnings | L7T10EIP3A |
| PM Toothache Relief | BENZOCAINE | Walgreens | e816f742-fba9-3c12-e053-2a95a90a192f | 2025-11-14 | Warnings | L7T10EIP3A |
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.