NDC 11004-502 - Dressol-X Radiopaque D-502
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
- 11004-502
- Package NDCs from labels
- 11004-502-40
- Manufacturer
- Rainbow Specialty & Health Products, Inc.
- Effective date
- 2011-12-13
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Dressol-X Radiopaque D-502 - Rainbow Specialty & Health Products, Inc. | Rainbow Specialty & Health Products, Inc. | 2011-12-13 | MEDICAL DEVICE |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 11004-502-40 | Dressol-XRadiopaque D-502 | 1 in 1 BOTTLE | DRESSING | 1 | 5 |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| ASPIRIN | ACTIVE INGREDIENT | R16CO5Y76E | DRESSOL-X RADIOPAQUE D-502 (ASPIRIN ) DRESSING [RAINBOW SPECIALTY & HEALTH PRODUCTS, INC.] | 5 | |
| EUGENOL | ACTIVE INGREDIENT | 3T8H1794QW | DRESSOL-X RADIOPAQUE D-502 (ASPIRIN ) DRESSING [RAINBOW SPECIALTY & HEALTH PRODUCTS, INC.] | 5 | |
| ASPIRIN | ACTIVE MOIETY | R16CO5Y76E | DRESSOL-X RADIOPAQUE D-502 (ASPIRIN ) DRESSING [RAINBOW SPECIALTY & HEALTH PRODUCTS, INC.] | 5 | |
| EUGENOL | ACTIVE MOIETY | 3T8H1794QW | DRESSOL-X RADIOPAQUE D-502 (ASPIRIN ) DRESSING [RAINBOW SPECIALTY & HEALTH PRODUCTS, INC.] | 5 | |
| MINERAL OIL | INACTIVE INGREDIENT | T5L8T28FGP | DRESSOL-X RADIOPAQUE D-502 (ASPIRIN ) DRESSING [RAINBOW SPECIALTY & HEALTH PRODUCTS, INC.] | 5 | |
| PARAFFIN | INACTIVE INGREDIENT | I9O0E3H2ZE | DRESSOL-X RADIOPAQUE D-502 (ASPIRIN ) DRESSING [RAINBOW SPECIALTY & HEALTH PRODUCTS, INC.] | 5 |
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.