NDC 41520-734-01 - CareOne Nicotine
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
- 41520-734
- Requested NDC
- 41520-734-01
- Package NDCs from labels
- 41520-734-01, 41520-734-02, 41520-734-03
- Manufacturer
- American Sales Company
- Effective date
- 2026-04-14
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| CareOne Nicotine - American Sales Company | American Sales Company | 2026-04-14 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 41520-734-01 | CareOne Nicotine | 27 in 1 CONTAINER | LOZENGE | 27 | 6 | |
| 41520-734-02 | CareOne Nicotine | 3 in 1 CARTON | LOZENGE | 3 | 6 | |
| 41520-734-03 | CareOne Nicotine | 4 in 1 CARTON | LOZENGE | 4 | 6 | |
| 41520-734-03 | CareOne Nicotine | 27 in 1 CONTAINER | LOZENGE | 27 | 6 |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| signature care nicotine | NICOTINE POLACRILEX | Safeway | 664c3faf-7cab-4bda-8987-07acb8e1142b | 2018-10-31 | Warnings | ANDA203690 6M3C89ZY6R |
| exchange select nicotine | NICOTINE POLACRILEX | Army & Air Force Exchange Service | e926cf6f-305a-4912-be07-a45bb7905822 | 2018-09-21 | Warnings | ANDA203690 6M3C89ZY6R |
| berkley and jensen nicotine | NICOTINE POLACRILEX | BJWC | 357123fc-0972-4683-ab52-f95d46c1b6c9 | 2017-11-09 | Warnings | ANDA203690 6M3C89ZY6R |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.