NDC 87118-005-01 - Esunix Oral Bacteriostatic Liquid
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
- 87118-005
- Requested NDC
- 87118-005-01
- Package NDCs from labels
- 87118-005-01, 87118-005-02
- Manufacturer
- Xiling (Zhenjiang) Medical Technology Co., Ltd.
- Effective date
- 2025-09-27
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Cetylpyridinium chloride - Xiling (Zhenjiang) Medical Technology Co., Ltd. | Xiling (Zhenjiang) Medical Technology Co., Ltd. | 2025-09-27 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 87118-005-01 | Esunix Oral Bacteriostatic Liquid | 12 mg in 1 BOX, UNIT-DOSE | LIQUID | 12 | 2 | |
| 87118-005-02 | Esunix Oral Bacteriostatic Liquid | 1 in 1 BOX | LIQUID | 1 | 2 |
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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| MENTHOL, CAMPHOR | MENTHOL, CAMPHOR | SUNSET NOVELTIES, INC | fc8a8f20-97ab-481e-e053-6394a90a3525 | 2025-11-20 | Warnings | L7T10EIP3A |
| MENTHOL | MENTHOL | SUNSET PAIN RELIEF ROLL-ON 3OZ | 934d4638-b47b-187d-e053-2995a90ae69d | 2025-11-20 | Warnings | L7T10EIP3A |
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| MENTHOL, CAMPHOR | MENTHOL, CAMPHOR | SUNSET PAIN RELIEF | 89f5f688-856f-f2df-e053-2995a90a73cf | 2025-11-19 | Warnings | L7T10EIP3A |
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.