Parasite Detox
- Product NDC
- 44911-0471
- Requested package NDC
- 44911-0471-1
- 11-digit product format
- 449110471
- Labeler code
- 44911
- Product ID
- 44911-0471_869e5bce-1ab2-457d-9113-5120b8f316b4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Granatum, Rhamnus Purshiana, Juglans Regia, Filix Mas, Absinthium, Aesculus Hippocastanum, Arsenicum Album, Baptisia Tinctoria, Cina, Cuprum Metallicum, Ipecacuanha, Lycopodium Clavatum, Mercurius Vivus, Nux Vomica, Pulsatilla (Vulgaris), Ratanhia, Rhus Tox, Sabadilla, Santoninum, Silicea, Spigelia Anthelmia, Teucrium Marum
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Energique, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2018-09-06
- Marketing end
- 2023-12-18
- Substance
- PUNICA GRANATUM ROOT BARK; FRANGULA PURSHIANA BARK; JUGLANS REGIA LEAF; DRYOPTERIS FILIX-MAS ROOT; WORMWOOD; HORSE CHESTNUT; ARSENIC TRIOXIDE; BAPTISIA TINCTORIA; ARTEMISIA CINA PRE-FLOWERING TOP; COPPER; IPECAC; LYCOPODIUM CLAVATUM SPORE; MERCURY; STRYCHNOS NUX-VOMICA SEED; PULSATILLA VULGARIS; KRAMERIA LAPPACEA ROOT; TOXICODENDRON PUBESCENS LEAF; SCHOENOCAULON OFFICINALE SEED; SANTONIN; SILICON DIOXIDE; SPIGELIA ANTHELMIA; TEUCRIUM MARUM
- 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; [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 | 44911-0471 | 44911-0471-1 | D | Discontinued by firm | 2026-09-14 |
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 |
|---|---|---|---|---|---|---|---|---|
| 44911-0471-1 | 44911047101 | 60 mL in 1 BOTTLE, DROPPER (44911-0471-1) | 60 ml | 2018-09-06 | 2023-12-18 | No | No | Current |