Petrochemical Detox
- Product NDC
- 43742-0915
- Requested package NDC
- 43742-0915-1
- 11-digit product format
- 437420915
- Labeler code
- 43742
- Product ID
- 43742-0915_122f7dfb-0f15-45fb-8d5a-06dc6994b107
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Chelidonium Majus, Symphytum Officinale, Taraxacum Officinale, Trifolium Pratense, Acetone, Sodium Tripolyphosphate, Propylene Glycol, Sodium Benzene Sulfonate, Ammonium Muriaticum, Sodium Lauryl Sulfate, Terebinthina, Arsenicum Album, Cadmium Sulphuratum, Gelsemium Sempervirens, Iridium Metallicum, Lycopodium Clavatum, Mercurius Solubilis, Nitricum Acidum, Nitricum Acidum, Nux Vomica, Petroleum, Phosphoricum Acidum, Platinum Metallicum, Latrodectus Mactans
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Deseret Biologicals, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2016-11-28
- Marketing end
- 2024-04-10
- Substance
- CHELIDONIUM MAJUS; TARAXACUM OFFICINALE; TRIFOLIUM PRATENSE FLOWER; COMFREY ROOT; ACETONE; AMMONIUM CHLORIDE; PROPYLENE GLYCOL; SODIUM BENZENESULFONATE; SODIUM LAURYL SULFATE; SODIUM TRIPOLYPHOSPHATE; TURPENTINE OIL; ARSENIC TRIOXIDE; CADMIUM SULFIDE; GELSEMIUM SEMPERVIRENS ROOT; IRIDIUM; LYCOPODIUM CLAVATUM SPORE; MERCURIUS SOLUBILIS; NITRIC ACID; STRYCHNOS NUX-VOMICA SEED; KEROSENE; PHOSPHORIC ACID; PLATINUM; LATRODECTUS MACTANS
- 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; [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 | 43742-0915 | 43742-0915-1 | 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 |
|---|---|---|---|---|---|---|---|---|
| 43742-0915-1 | 43742091501 | 30 mL in 1 BOTTLE, DROPPER (43742-0915-1) | 30 ml | 2016-11-28 | 2024-04-10 | No | No | Current |