NDC 10210-0038-01 - Carmex Classic Lip Balm Medicated
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
- 10210-0038
- Requested NDC
- 10210-0038-01
- Package NDCs from labels
- 10210-0038-1, 10210-0038-0, 10210-0038-01
- Manufacturer
- Carma Laboratories, Inc.
- Effective date
- 2026-01-09
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Carmex Classic Lip Balm Medicated | Carma Laboratories, Inc. | 2026-01-09 | HUMAN OTC DRUG LABEL |
| Carmex Classic Lip Balm Medicated Free Wintergreen Stick, kit | Carma Laboratories, Inc. | 2023-12-08 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 10210-0038-1 | Carmex Classic Lip Balm Medicated | 4 in 1 TRAY | SALVE | 4 | 4 | |
| 10210-0038-1 | Carmex Classic Lip Balm Medicated | 10 g in 1 TUBE | SALVE | 10 | 4 | |
| 10210-0038-0 | Carmex Classic Lip Balm Medicated Free Wintergreen Stick | 10 g in 1 TUBE | SALVE | 10 g | 453 mg in 1g | 3 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 10210-0038 | CARMEX CLASSIC LIP BALM MEDICATED (CAMPHOR (SYNTHETIC), WHITE PETROLATUM) SALVE [CARMA LABORATORIES, INC.] | 3 | Current NDC, Legacy NDC, 2 package rows | 20231026_bb0278c9-eaff-d435-e053-2995a90a202a.zip |
| 10210-0038 | CARMEX CLASSIC LIP BALM MEDICATED FREE WINTERGREEN STICK (OCTINOXATE, OXYBENZONE, CAMPHOR (SYNTHETIC), WHITE PETROLATUM) KIT [CARMA LABORATORIES, INC.] | 3 | Current NDC, Legacy NDC | 20231209_bc0162bc-92ca-ee78-e053-2a95a90a7c9d.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.