Rheumatic Tonic
- Product NDC
- 43857-0448
- Requested package NDC
- 43857-0448-1
- 11-digit product format
- 438570448
- Labeler code
- 43857
- Product ID
- 43857-0448_1af85379-fd68-43c9-86e9-d841b589ae76
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Harpagophytum Procumbens, Symphytum Officinale, Salix Alba, Colchicum Autumnale, Pinus Sylvestris, Aconitum Napellus, Arnica Montana, Gelsemium Sempervirens, Iris Versicolor, Ledum Palustre, Lespedeza Capitata, Rhus Tox, Secale Cornutum, Spigelia Anthelmia, Spiraea Ulmaria, Tartaricum Acidum
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- BioActive Nutritional, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2017-06-06
- Marketing end
- 2022-07-12
- Substance
- HARPAGOPHYTUM PROCUMBENS ROOT; SALIX ALBA BARK; COLCHICUM AUTUMNALE BULB; PINUS SYLVESTRIS LEAFY TWIG; COMFREY ROOT; ACONITUM NAPELLUS; ARNICA MONTANA; GELSEMIUM SEMPERVIRENS ROOT; IRIS VERSICOLOR ROOT; LEDUM PALUSTRE TWIG; LESPEDEZA CAPITATA FLOWERING TOP; TOXICODENDRON PUBESCENS LEAF; CLAVICEPS PURPUREA SCLEROTIUM; SPIGELIA ANTHELMIA; FILIPENDULA ULMARIA ROOT; TARTARIC ACID
- Active strength
- 1 [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; [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 | 43857-0448 | 43857-0448-1 | 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 | Snapshot | Source SHA-256 |
|---|---|---|
| 2025-12-14 17:58 UTC · source 2025-12-05 | d630ba8d3edf… | 732f749b63fb… |
| 2025-08-27 00:01 UTC · source 2025-08-26 | f5e01cc5f278… | a2eaf40c39c3… |
| 2025-04-01 02:39 UTC · source 2025-03-31 | 2ef7874e63bc… | 57b86245f4fa… |
| 2025-03-28 20:22 UTC · source 2025-03-28 | a1b67e2a42f9… | c4cf2c586c0d… |
| 2025-03-22 03:12 UTC · source 2025-03-21 | cfe11265f3b6… | 090c488252e2… |
| 2025-03-10 12:48 UTC · source 2025-03-10 | cdf11ea48f46… | ba0047e9e063… |
| 2025-02-02 03:52 UTC · source 2025-01-31 | 302b2466d912… | e7b80fea0513… |
| 2025-01-20 13:05 UTC · source 2025-01-20 | ed331223b511… | 672a5bd82f5f… |
| 2025-01-11 03:41 UTC · source 2025-01-10 | 0efc9e666f02… | f202fb6c5f17… |
| 2024-11-09 02:27 UTC · source 2024-11-08 | ad56d346431e… | cc804d4bbf1e… |
| 2024-10-04 04:10 UTC · source 2024-10-03 | 367a005e9d99… | 383a685ebd0f… |
| 2024-07-10 04:00 UTC · source 2024-07-09 | 557ba5c1ecfa… | 9c80585c8c6e… |
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 |
|---|---|---|---|---|---|---|---|---|
| 43857-0448-1 | 43857044801 | 60 mL in 1 BOTTLE, DROPPER (43857-0448-1) | 60 ml | 2017-06-06 | 2022-07-12 | No | No | Current |