Arrhythmiaforce
- Product NDC
- 43857-0556
- Requested package NDC
- 43857-0556-1
- 11-digit product format
- 438570556
- Labeler code
- 43857
- Product ID
- 43857-0556_fc5c9f14-3bd5-4a96-986a-b57d6db6522f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Juglans Nigra, Leonurus Cardiaca, Convallaria Majalis, Magnesia Sulphurica, Iberis Amara, Kali Chloricum, Adonis Vernalis, Digitalis Purpurea, Lycopus Virginicus, Phosphorus
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- BioActive Nutritional, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2020-04-27
- Marketing end
- 2025-05-14
- Substance
- BLACK WALNUT; LEONURUS CARDIACA WHOLE; CONVALLARIA MAJALIS; MAGNESIUM SULFATE HEPTAHYDRATE; IBERIS AMARA SEED; POTASSIUM CHLORATE; ADONIS VERNALIS WHOLE; DIGITALIS; LYCOPUS VIRGINICUS WHOLE; PHOSPHORUS
- Active strength
- 3 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded package | package | 43857-0556 | 43857-0556-1 | D | Discontinued by firm | 2026-10-05 |
Observed NDC auxiliary status history#
This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
| Captured / source date | Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Archive | Snapshot | Source SHA-256 |
|---|---|---|---|---|---|---|---|---|---|---|
| 2025-12-14 17:58 UTC · source 2025-12-05 | excluded package | package | 43857-0556 | 43857-0556-1 | D | Discontinued by firm | excluded / ndc_excluded.zip | d630ba8d3edf… | 732f749b63fb… | |
| 2025-08-27 00:01 UTC · source 2025-08-26 | excluded package | package | 43857-0556 | 43857-0556-1 | D | Discontinued by firm | excluded / ndc_excluded.zip | f5e01cc5f278… | a2eaf40c39c3… |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 43857-0556-1 | 43857055601 | 30 mL in 1 BOTTLE, DROPPER (43857-0556-1) | 30 ml | 2020-04-27 | 2025-05-14 | No | No | Current |