Aconitum e tub. 30
- Product NDC
- 48951-1338
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aconitum e tub. 30
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Substance
- ACONITUM NAPELLUS
- Current FDA listing
- Yes
Related Records
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|---|---|---|---|---|
| 48951-1338-1 | 10 AMPULE in 1 BOX (48951-1338-1) / 1 mL in 1 AMPULE | 2009-09-01 | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|---|---|---|---|
| Aconitum e tub. 30 | Uriel Pharmacy Inc. | 2025-11-06 | HUMAN OTC DRUG LABEL | 7 |
| Aconitum e tub. 30 | Uriel Pharmacy Inc. | 2021-07-07 | HUMAN OTC DRUG LABEL | 6 |