NDC 52124-0014 - CVS First Aid Kit
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
- 52124-0014
- Package NDCs from labels
- 52124-0014-1
- Manufacturer
- CVS | Tender Corporation
- Effective date
- 2017-01-18
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| CVS First Aid Kit - CVS | Tender Corporation | CVS | Tender Corporation | 2017-01-18 | HUMAN OTC DRUG LABEL |
| CVS Health Medication and Topical Refill Pouch - CVS | Tender Corporation | CVS | Tender Corporation | 2017-01-18 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 52124-0014-1 | CVS First Aid Kit | 2 in 1 PACKAGE | TABLET | 2 | 500 mg | 2 |
| 52124-0014-1 | CVS Health Medication and Topical Refill Pouch | 2 in 1 PACKAGE | TABLET | 2 | 500 mg | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 52124-0014 | CVS FIRST AID KIT (DIPHENHYDRAMINE HYDROCHLORIDE, ASPIRIN, ISOPROPYL ALCOHOL, BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B, BENZALKONIUM CHLORIDE, AMMONIA, LIDOCAINE, ACETAMINOPHEN, IBUPROFEN,) KIT [CVS] | 2 | Unmatched | 20170118_44bc7046-4a72-7085-e054-00144ff8d46c.zip |
| 52124-0014 | CVS HEALTH MEDICATION AND TOPICAL REFILL POUCH (ASPIRIN, DIPHENHYDRAMINE HYDROCHLORIDE, ASPIRIN, ISOPROPYL ALCOHOL, BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B, ACETAMINOPHEN) KIT [CVS] | 1 | Unmatched | 20170119_4664c90e-276e-0f6e-e054-00144ff88e88.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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.