NDC 67172-019 - Chloraseptic Warming Honey Lemon
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
- 67172-019
- Package NDCs from labels
- 67172-019-02
- Manufacturer
- Prestige Brands Holdings, Inc.
- Effective date
- 2025-09-08
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| CORN SYRUP - Prestige Brands Holdings, Inc. | Prestige Brands Holdings, Inc. | 2025-09-08 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 67172-019-02 | Chloraseptic Warming Honey Lemon | 18 in 1 CARTON | LOZENGE | 18 | 3 |
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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| CLENZIDERM THERAPEUTIC MOISTURIZER | GLYCERIN | Obagi Cosmeceuticals LLC | d60e22e3-831e-4787-a82c-e7763c287553 | 2025-01-01 | Warnings | PDC6A3C0OX |
| Rite Aid Hydration Lubricant Eye Drops | POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL | Rite Aid Corporation | ecac1351-e944-21da-e053-2995a90a6d34 | 2024-12-31 | Warnings | 6DC9Q167V3 |
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| Mirakel Pain and Itch Relief | BENZOCAINE 20%, RESORCINOL 3% | Sanvio, Inc. | ed34d728-0275-e209-e053-2995a90a93ff | 2024-12-20 | Warnings | U3RSY48JW5 |
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| Pain, Burn, and Itch Relief | BENZOCAINE 20%, MENTHOL 0.5% | Derma Care Research Labs, LLC | fd9fe09f-3ae9-c5f5-e053-6394a90ad691 | 2024-12-19 | Warnings | U3RSY48JW5 |
| Revivol Hemorrhoid and Fissure | GLYCERIN 14.4%, LIDOCAINE 5%, PETROLATUM 15%, PHENYLEPHRINE HCL 0.25% | Derma Care Research Labs, LLC | 0140cf68-b6a0-4378-e063-6394a90afee8 | 2024-12-19 | Warnings | PDC6A3C0OX |
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.