NDC 65753-101-10 - CoreTex Sun X SPF 30 Thin
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
- 65753-101
- Requested NDC
- 65753-101-10
- Package NDCs from labels
- 65753-101-11, 65753-101-12, 65753-101-27, 65753-101-22, 65753-101-23, 65753-101-24, 65753-101-25, 65753-101-26, 65753-101-10
- Manufacturer
- CoreTex Products Inc | Pure Source
- Effective date
- 2023-10-22
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| CoreTex Sun X SPF 30 Thin - CoreTex Products Inc | Pure Source | CoreTex Products Inc | Pure Source | 2023-10-22 | HUMAN OTC DRUG LABEL |
| SunX SPF 30/BugX Wallmount - CoreTex Products Inc | Pure Source | CoreTex Products Inc | Pure Source | 2023-10-22 | HUMAN OTC DRUG LABEL |
| SunX SPF 30/BugX Wallmount - CoreTex Products Inc | Pure Source | CoreTex Products Inc | Pure Source | 2023-10-11 | HUMAN OTC DRUG LABEL |
| SunX SPF 30/BugX Wallmount - CoreTex Products Inc | Pure Source | CoreTex Products Inc | Pure Source | 2022-11-21 | HUMAN OTC DRUG LABEL |
| SunX SPF 30/BugX Wallmount - CoreTex Products Inc | Pure Source | CoreTex Products Inc | Pure Source | 2022-11-21 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 65753-101-11 | CoreTex Sun X SPF 30 Thin | 59 mL in 1 BOTTLE, SPRAY | LIQUID | 59 | 6 | |
| 65753-101-12 | CoreTex Sun X SPF 30 Thin | 118 mL in 1 BOTTLE, SPRAY | LIQUID | 118 | 6 | |
| 65753-101-22 | CoreTex Sun X SPF 30 Thin | 7 mL in 1 PACKET | LIQUID | 7 | 6 | |
| 65753-101-22 | CoreTex Sun X SPF 30 Thin | 25 in 1 CONTAINER | LIQUID | 25 | 6 | |
| 65753-101-23 | CoreTex Sun X SPF 30 Thin | 50 in 1 CONTAINER | LIQUID | 50 | 6 | |
| 65753-101-23 | CoreTex Sun X SPF 30 Thin | 7 mL in 1 PACKET | LIQUID | 7 | 6 | |
| 65753-101-24 | CoreTex Sun X SPF 30 Thin | 50 in 1 CARTON | LIQUID | 50 | 6 | |
| 65753-101-24 | CoreTex Sun X SPF 30 Thin | 7 mL in 1 PACKET | LIQUID | 7 | 6 | |
| 65753-101-25 | CoreTex Sun X SPF 30 Thin | 100 in 1 CARTON | LIQUID | 100 | 6 | |
| 65753-101-25 | CoreTex Sun X SPF 30 Thin | 7 mL in 1 PACKET | LIQUID | 7 | 6 | |
| 65753-101-26 | CoreTex Sun X SPF 30 Thin | 300 in 1 BOX | LIQUID | 300 | 6 | |
| 65753-101-26 | CoreTex Sun X SPF 30 Thin | 7 mL in 1 PACKET | LIQUID | 7 | 6 | |
| 65753-101-27 | CoreTex Sun X SPF 30 Thin | 7 mL in 1 PACKET | LIQUID | 7 | 6 | |
| 65753-101-27 | CoreTex Sun X SPF 30 Thin | 16 in 1 BOX | LIQUID | 16 | 6 | |
| 65753-101-10 | SunX SPF 30/BugX Wallmount | 7 mL in 1 POUCH | LIQUID | 350 mL | 7.5 g in 100mL | 1 |
| 65753-101-10 | SunX SPF 30/BugX Wallmount | 7 mL in 1 POUCH | LIQUID | 350 mL | 7.5 g in 100mL | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 65753-101 | CORETEX SUN X SPF 30 THIN (AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE, OXYBENZONE) LIQUID [CORETEX PRODUCTS INC] | 6 | Current NDC, Legacy NDC, 14 package rows | 20231022_980388b5-8314-3143-e053-2995a90a7288.zip |
| 65753-101 | SUNX SPF 30/BUGX WALLMOUNT KIT [CORETEX PRODUCTS INC] | 1 | Current NDC, Legacy NDC | 20231022_0846946b-a05d-826c-e063-6294a90a0a0f.zip |
| 65753-101 | SUNX SPF 30/BUGX WALLMOUNT KIT [CORETEX PRODUCTS INC] | 1 | Current NDC, Legacy NDC | 20231022_08480b2a-a888-fb00-e063-6294a90a41ea.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.