Home NDC 70321-0003-1 Energize
Product NDC 70321-0003
Requested package NDC 70321-0003-1
11-digit product format 703210003
Labeler code 70321
Product ID 70321-0003_a135565d-8c93-458b-ad68-3aab3acb954d
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, Thiaminum Hydrochloricum, Norepinephrine, Alpha-Lipoicum Acidum, Natrum Oxalaceticum, Sulphur, Acetylsalicylicum Acidum, Adenosinum Triphosphoricum Dinatrum, Anthrachinonum, Histaminum Hydrochloricum, Magnesium Gluconicum Dihydricum, Nadidum, Naphthochinonum, Pantothenic Acid
Dosage form LIQUID
Route ORAL
Labeler Parasitology Center Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2016-04-27
Marketing end 0000-00-00
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; BACILLUS ANTHRACIS IMMUNOSERUM RABBIT; HISTAMINE DIHYDROCHLORIDE; MAGNESIUM GLUCONATE; NADIDE; 1,4-NAPHTHOQUINONE; PANTOTHENIC ACID; UBIDECARENONE; MANGANESE PHOSPHATE, DIBASIC; HYDROQUININE; SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS
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 2020-12-31
Current FDA listing Historical FDA.report record 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.
Historic NDC status page 1 of 1 · 2 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 70321-0003 70321-0003-1 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 70321-0003 70321-0003-1 D Discontinued by firm excluded / ndc_excluded.zip f5e01cc5f278…a2eaf40c39c3…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70321-0003 ENERGIZE (COLCHICUM AUTUMNALE, CONIUM MACULATUM, HYDRASTIS CANADENSIS, VACCINIUM MYRTILLUS, PODOPHYLLUM PELTATUM, ASCORBIC ACID, GALIUM APARINE, NICOTINAMIDUM, PYRIDOXINUM HYDROCHLORICUM, RIBOFLAVINUM, SARCOLACTICUM ACIDUM, THIAMINUM HYDROCHLORICUM, NOREPINEPHRINE, ALPHA-LIPOICUM ACIDUM, NATRUM OXALACETICUM, SULPHUR, ACETYLSALICYLICUM ACIDUM, ADENOSINUM TRIPHOSPHORICUM DINATRUM, ANTHRACHINONUM, HISTAMINUM HYDROCHLORICUM, MAGNESIUM GLUCONICUM DIHYDRICUM, NADIDUM, NAPHTHOCHINONUM, PANTOTHENIC ACID) LIQUID [PARASITOLOGY CENTER INC.] 2 Legacy NDC 20250523_1228bfab-6e51-4295-8194-5f2b395d62d2.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 70321-0003-1 70321000301 30 mL in 1 BOTTLE, DROPPER (70321-0003-1) 30 ml 2016-04-27 0000-00-00 No No Current