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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| Flexigen | MENTHOL 1.25% | Derma Care Research Labs, LLC | e9ae2682-59b4-e796-e053-2995a90af921 | 2024-01-15 | Warnings | L7T10EIP3A |
| Vita-P Oral and Nasal | MENTHOL 1% | Beijing HKKY Medical Tech. Co., Ltd. | 537c3843-1c92-41c6-b724-52701bbddeab | 2024-01-13 | Warnings | L7T10EIP3A |
| Cool n Heat | COOL N HEAT | NeilMed Pharmaceuticals, Inc. | a24cde17-280b-8358-e053-2a95a90af67d | 2024-01-11 | Warnings | L7T10EIP3A |
| NeilMed Hot and Cold Pain Relief | PAIN RELIEF SPRAY | NeilMed Pharmaceuticals Inc. | b3d02111-7499-c2d4-e053-2a95a90ae1de | 2024-01-11 | Warnings | L7T10EIP3A |
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| MED O-3 BIO- | METHYL SALICYLATE, MENTHOL, CAPSAICIN | Biological M.D. Solutions LLC | 02707552-03d9-3ad2-e063-6294a90a3472 | 2024-01-06 | Warnings | L7T10EIP3A |
| Fendall 2000 Pure Flow | PURIFIED WATER | Honeywell Safety Products USA, Inc. | b56ef662-fec2-4d94-e053-2995a90aba2b | 2024-01-06 | Warnings | 059QF0KO0R |
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| OWELL NATURALS Deep Penetrating Pain Relief | MENTHOL | OWELL NATURALS BRAND, LLC | b36eb017-ed8d-476e-994b-22b275e00543 | 2024-01-02 | Warnings | L7T10EIP3A |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.