NDC 73096-028-01 - Flexible Pain Relief Gel Extra Strength
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
- 73096-028
- Requested NDC
- 73096-028-01
- Package NDCs from labels
- 73096-028-01, 73096-028-02
- Manufacturer
- ABACUS HEALTH PRODUCTS, INC. | Inspec Solutions LLC.
- Effective date
- 2021-12-31
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Flexible Pain Relief Gel Extra Strength | ABACUS HEALTH PRODUCTS, INC. | Inspec Solutions LLC. | 2021-12-31 | HUMAN OTC DRUG LABEL |
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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| LIDOTHOL | LIDOCAINE AND MENTHOL | Advanced Rx Pharmacy of Tennessee, LLC | 181f0806-dab7-410c-e063-6294a90ac09c | 2024-05-10 | Warnings, Adverse reactions | L7T10EIP3A |
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| Fleet | GLYCERIN | C.B. Fleet Company, Inc. | 381f4179-0c3b-41f8-927c-c88534ebe06d | 2024-05-06 | Warnings | PDC6A3C0OX |
| Professional Therapy MuscleCare Pro Pain Relieving Cold Gel | CAMPHOR, MENTHOL | ACTIVE AND INNOVATIVE, LLC | 1794c512-5f42-4ec3-e063-6394a90a87cd | 2024-05-03 | Warnings | L7T10EIP3A |
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| Professional Therapy MuscleCare Pro Roll-on | CAMPHOR, MENTHOL | ACTIVE AND INNOVATIVE, LLC | 1755ec89-c404-1c17-e063-6394a90ab9fb | 2024-04-30 | Warnings | L7T10EIP3A |
| PAIN RELIEF Gel-Roll On | MENTHOL | Shanghai Chuangshi Medical Technology (Group) Co., Ltd. | f0bc2a14-6bda-428c-e053-2995a90a4ced | 2024-04-29 | Warnings | L7T10EIP3A |
| PAIN RELIEF Gel-Tube | MENTHOL | Shanghai Chuangshi Medical Technology (Group) Co., Ltd. | f0bec1d4-2e18-4519-e053-2a95a90a1bbb | 2024-04-29 | Warnings | L7T10EIP3A |
| Eucalyptus globulus | EUCALYPTUS GLOBULUS LEAF | Boiron | 16f13c97-0915-a642-e063-6294a90a209c | 2024-04-25 | S546YLW6E6 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.