Energize
- Product NDC
- 70321-0001
- Requested package NDC
- 70321-0001-1
- 11-digit product format
- 703210001
- Labeler code
- 70321
- Product ID
- 70321-0001_b3774d72-5888-44cc-880c-cabd4217713e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Colchicum Autumnale, Conium Maculatum, Hydrastis Canadensis, Vaccinium Myrtillus, Podophyllum Peltatum, Ascorbic Acid, Galium Aparine, Nicotinamidum, Pyridoxinum Hydrochloricum, Riboflavinum, Sarcolacticum Acidum, Norepinephrine, Alpha-Lipoicum Acidum, Natrum Oxalaceticum, Sulphur, Acetylsalicylicum Acidum, Anthraquinone, Coenzyme A, Histaminum Hydrochloricum, Magnesium Gluconate, Nadidum, Naphthoquinone, Ubidecarenonum, Magnesium Phosphoricum, Hydroquinone, Morgan Gaertner
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Parasitology Center, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2016-03-10
- Marketing end
- 2021-03-23
- Substance
- COLCHICUM AUTUMNALE BULB; CONIUM MACULATUM FLOWERING TOP; GOLDENSEAL; BILBERRY; PODOPHYLLUM; ASCORBIC ACID; GALIUM APARINE; NIACINAMIDE; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN; LACTIC ACID, L-; THIAMINE HYDROCHLORIDE; NOREPINEPHRINE; THIOCTIC ACID; SODIUM DIETHYL OXALACETATE; SULFUR; ASPIRIN; ADENOSINE TRIPHOSPHATE DISODIUM; ANTHRAQUINONE; COENZYME A; HISTAMINE DIHYDROCHLORIDE; MAGNESIUM GLUCONATE; NADIDE; 1,4-NAPHTHOQUINONE; UBIDECARENONE; MANGANESE PHOSPHATE, DIBASIC; HYDROQUINONE; PROTEUS MORGANII
- Active strength
- 4 [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; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/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 | 70321-0001 | 70321-0001-1 | D | Discontinued by firm | 2026-10-12 |
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 |
|---|---|---|---|---|---|---|---|---|
| 70321-0001-1 | 70321000101 | 30 mL in 1 BOTTLE, DROPPER (70321-0001-1) | 30 ml | 2016-03-10 | 2021-03-23 | No | No | Current |