Fire Opal
- Product NDC
- 63083-8117
- 11-digit product format
- 630838117
- Labeler code
- 63083
- Product ID
- 63083-8117_33aea71c-33f8-412c-a1fe-43492c2e89cb
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Fire Opal
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Professional Complementary Health Formulas
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 1984-08-15
- Marketing end
- 0000-00-00
- Substance
- EPOXICONAZOLE
- Active strength
- 6 [hp_X]/59mL
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| U80T84L776 | EPOXICONAZOLE | 133855-98-8 | EPOXICONAZOLE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63083-8117-2 | 63083811702 | 59 mL in 1 BOTTLE, DROPPER (63083-8117-2) | 59 ml | 1985-08-15 | 0000-00-00 | No | No | Current |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| UFO | Professional Complementary Health Formulas | Natural Pharmaceutical Manufacturing LLC | 2019-08-15 | HUMAN OTC DRUG LABEL | 1 |