Chemtox
- Product NDC
- 73518-0001
- Requested package NDC
- 73518-0001-1
- 11-digit product format
- 735180001
- Labeler code
- 73518
- Product ID
- 73518-0001_fbabcb86-64c3-4874-a92d-8a15e1e2ebea
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Berberis Vulgaris, Taraxacum Officinale, Ammonium Carbonicum, Camphora, Cysteinum, Nux Vomica, Sulphuricum Acidum, Acetaldehyde, Benzinum, Calcarea Carbonica, Carbolicum Acidum, Kreosotum, Lachesis Mutus, Naphthalinum, Plumbum Metallicum, Formalinum, Carboneum Chloratum, Chloroformum, Etherum, Paraffinum, Petroleum
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Energenx LLC
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2020-07-14
- Marketing end
- 0000-00-00
- Substance
- BERBERIS VULGARIS ROOT BARK; TARAXACUM OFFICINALE; AMMONIUM CARBONATE; CAMPHOR (NATURAL); CYSTEINE; STRYCHNOS NUX-VOMICA SEED; SULFURIC ACID; ACETALDEHYDE; BENZENE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; PHENOL; WOOD CREOSOTE; LACHESIS MUTA VENOM; NAPHTHALENE; LEAD; FORMALDEHYDE SOLUTION; CARBON TETRACHLORIDE; CHLOROFORM; ETHER; PARAFFIN; KEROSENE
- 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
- 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 | 73518-0001 | 73518-0001-1 | 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 |
|---|---|---|---|---|---|---|---|---|
| 73518-0001-1 | 73518000101 | 60 mL in 1 BOTTLE, DROPPER (73518-0001-1) | 60 ml | 2020-07-14 | 0000-00-00 | No | No | Current |