NDC 10210-0035 - Carmex Variety Pack Daily Care Moisturizing Lip Balm SPF 15
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
- 10210-0035
- Package NDCs from labels
- 10210-0035-0
- Manufacturer
- Carma Laboratories, Inc.
- Effective date
- 2026-10-02
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Carmex Variety Pack - Daily Care Moisturizing Lip Balm SPF 15 | Carma Laboratories, Inc. | 2026-10-02 | HUMAN OTC DRUG LABEL |
| Carmex Variety Pack - Daily Care Moisturizing Lip Balm SPF 15 | Carma Laboratories, Inc. | 2026-10-02 | HUMAN OTC DRUG LABEL |
| OCTINOXATE, OXYBENZONE - Carma Laboratories, Inc. | Carma Laboratories, Inc. | 2023-10-25 | HUMAN OTC DRUG LABEL |
| Carmex Daily Care Moisturizing Lip Balm SPF 15 Minis, Kit | Carma Laboratories, Inc. | 2023-10-25 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 10210-0035-0 | Carmex Daily Care Moisturizing Lip Balm SPF 15 Sunscreen Minis | 5 g in 1 TUBE | SALVE | 5 g | 75 mg in 1g | 2 |
| 10210-0035-0 | Carmex Daily Care Moisturizing Lip Balm SPF 15 Minis | 5 g in 1 TUBE | SALVE | 5 g | 75 mg in 1g | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 10210-0035 | CARMEX DAILY CARE MOISTURIZING LIP BALM SPF 15 MINIS (OCTINOXATE, OXYBENZONE) KIT [CARMA LABORATORIES, INC.] | 2 | Unmatched | 20231026_bb029c71-4f07-2754-e053-2995a90a7c78.zip |
| 10210-0035 | CARMEX DAILY CARE MOISTURIZING LIP BALM SPF 15 SUNSCREEN MINIS (OCTINOXATE, OXYBENZONE) KIT [CARMA LABORATORIES, INC.] | 2 | Unmatched | 20231026_4e868b1a-7c47-45de-83cd-0bd5fbb05a27.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.