HBP
- Product NDC
- 55714-4841
- Requested package NDC
- 55714-4841-1
- 11-digit product format
- 557144841
- Labeler code
- 55714
- Product ID
- 55714-4841_a606438c-7b10-4b1a-e053-2a95a90ad46f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ruta graveolens, Valeriana officinalis, Adrenalinum, Arsenicum iodatum, Aurum metallicum, Baryta carbonica, Bryonia, Cactus grandiflorus, Chelidonium majus, Cinchona officinalis, Crotalus horridus, Digitalis purpurea, Glonoinum, Kali carbonicum, Kali iodatum, Lachesis mutus, Naja tripudians, Nux vomica, Veratrum album, Vipera berus, Viscum album, Elaps corallinus.
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Newton Laboratories, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2020-05-18
- Marketing end
- 0000-00-00
- Substance
- MICRURUS CORALLINUS VENOM; VISCUM ALBUM FRUITING TOP; RUTA GRAVEOLENS FLOWERING TOP; VIPERA BERUS VENOM; EPINEPHRINE; ARSENIC TRIIODIDE; GOLD; BARIUM CARBONATE; BRYONIA ALBA ROOT; SELENICEREUS GRANDIFLORUS STEM; CHELIDONIUM MAJUS; CINCHONA OFFICINALIS BARK; CROTALUS HORRIDUS HORRIDUS VENOM; DIGITALIS; NITROGLYCERIN; POTASSIUM CARBONATE; POTASSIUM IODIDE; LACHESIS MUTA VENOM; NAJA NAJA VENOM; STRYCHNOS NUX-VOMICA SEED; VERATRUM ALBUM ROOT; VALERIAN
- Active strength
- 30 [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; [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
- 2021-12-31
- 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 | 55714-4841 | 55714-4841-1 | 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 |
|---|---|---|---|---|---|---|---|---|
| 55714-4841-1 | 55714484101 | 30 mL in 1 BOTTLE, GLASS (55714-4841-1) | 30 ml | 2020-05-18 | 0000-00-00 | No | No | Current |