NDC 10157-1120-03 - Blistex Medicated Mint Balm
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
- 10157-1120
- Requested NDC
- 10157-1120-03
- Package NDCs from labels
- 10157-1120-1, 10157-1120-2, 10157-1120-3, 10157-1120-4, 10157-1120-03
- Manufacturer
- Blistex Inc
- Effective date
- 2024-02-09
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Blistex Medicated Mint Balm - Blistex Inc | Blistex Inc | 2024-02-09 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 10157-1120-1 | Blistex Medicated Mint Balm | 4.25 g in 1 CYLINDER | STICK | 4.25 | 3 | |
| 10157-1120-1 | Blistex Medicated Mint Balm | 1 in 1 CARTON | STICK | 1 | 3 | |
| 10157-1120-2 | Blistex Medicated Mint Balm | 4.25 g in 1 CYLINDER | STICK | 4.25 | 3 | |
| 10157-1120-2 | Blistex Medicated Mint Balm | 2 in 1 CARTON | STICK | 2 | 3 | |
| 10157-1120-3 | Blistex Medicated Mint Balm | 3 in 1 CARTON | STICK | 3 | 3 | |
| 10157-1120-3 | Blistex Medicated Mint Balm | 4.25 g in 1 CYLINDER | STICK | 4.25 | 3 | |
| 10157-1120-4 | Blistex Medicated Mint Balm | 4 in 1 CARTON | STICK | 4 | 3 | |
| 10157-1120-4 | Blistex Medicated Mint Balm | 4.25 g in 1 CYLINDER | STICK | 4.25 | 3 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 10157-1120 | BLISTEX MEDICATED MINT BALM (DIMETHICONE, OCTINOXATE, AND OCTISALATE) STICK [BLISTEX INC] | 3 | Current NDC, Legacy NDC, 8 package rows | 20240214_86fc9f3c-e35f-4988-bf19-64d9c6c85ee9.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.