Azurite
- Product NDC
- 63083-8106
- 11-digit product format
- 630838106
- Labeler code
- 63083
- Product ID
- 63083-8106_7ea97a44-435d-4a77-9147-cc8fc82d2869
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Azurite
- 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
- AZURITE
- 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 |
|---|
| 9AD6E582QL | AZURITE | 1319-45-5 | AZURITE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63083-8106-2 | 63083810602 | 59 mL in 1 BOTTLE, DROPPER (63083-8106-2) | 59 ml | 1985-08-15 | 0000-00-00 | No | No | Current |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| UAZU | Professional Complementary Health Formulas | Natural Pharmaceutical Manufacturing LLC | 2019-08-15 | HUMAN OTC DRUG LABEL | 1 |