NDC 79481-0087-01 - meijer Cold Therapy Pain Relieving analgesic
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
- 79481-0087
- Requested NDC
- 79481-0087-01
- Package NDCs from labels
- 79481-0087-1, 79481-0087-01
- Manufacturer
- Meijer Distribution, Inc | Garcoa, Inc. | SV Labs Toronto Corporation
- Effective date
- 2024-02-28
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| meijer ® Cold Therapy Pain Relieving Gel Topical analgesic | Meijer Distribution, Inc | Garcoa, Inc. | SV Labs Toronto Corporation | 2024-02-28 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 79481-0087-1 | meijer Cold Therapy Pain Relievinganalgesic | 89 mL in 1 TUBE | GEL | 89 | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 79481-0087 | MEIJER COLD THERAPY PAIN RELIEVING ANALGESIC (MENTHOL, UNSPECIFIED FORM) GEL [MEIJER DISTRIBUTION, INC] | 1 | Current NDC, 1 package rows | 20240301_fb163112-d84d-418d-a410-3214c0ee4b5a.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.
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| Eagle Brand Medicated Roll On Refresh | CAMPHOR, MENTHOL | PT. EAGLE INDO PHARMA | 09235f26-2262-6ca2-e063-6394a90ad8f1 | 2026-04-27 | Warnings | M017 L7T10EIP3A 5TJD82A1ET |
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| REFRESH TEARS PF | CARBOXYMETHYLCELLULOSE SODIUM, GLYCERIN | Allergan, Inc. | 9e1cba7b-84ed-47f3-b19a-121992834350 | 2026-04-24 | Warnings | PDC6A3C0OX |
| HIP PAIN RELIEF ROLL-ON | LIDOCAINE AND MENTHOL | Guangzhou Liuquanmiao Import & Export Trade Co., Ltd. | 502f1f9e-8552-ca7b-e063-6394a90a7c53 | 2026-04-24 | Warnings | M017 L7T10EIP3A |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.