Ultra Advantage

Product NDC

69719-0001

11-digit product format

697190001

Labeler code

69719

Product ID

69719-0001_4482a3fa-84d1-4cb0-97c1-9cf03db49e9f

Type

HUMAN OTC DRUG

Nonproprietary name

Abrotanum (Artemisia Abrotanum), Anacardium Orientale, Baryta Muriatica, Calcarea Carbonica, Calcarea Phosphorica, Fucus Vesiculosus, Graphites, Helleborus Niger, Hypothalamus (Suis), Ignatia Amara, Lycopodium Clavatum, Magnesia Phosphorica, Secale Cornutum, Silicea, Thymus Serpyllum, Thyroidinum (Suis), Solidago Virgaurea

Dosage form

LIQUID

Route

ORAL

Labeler

Soza Weight Loss LLC

Marketing category

UNAPPROVED HOMEOPATHIC

Marketing start

2015-04-28

Marketing end

2022-05-20

Substance

ARTEMISIA ABROTANUM FLOWERING TOP; BARIUM CHLORIDE DIHYDRATE; CLAVICEPS PURPUREA SCLEROTIUM; FUCUS VESICULOSUS; GRAPHITE; HELLEBORUS NIGER ROOT; LYCOPODIUM CLAVATUM SPORE; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; SEMECARPUS ANACARDIUM JUICE; SILICON DIOXIDE; SOLIDAGO VIRGAUREA FLOWERING TOP; STRYCHNOS IGNATII SEED; SUS SCROFA HYPOTHALAMUS; SUS SCROFA THYROID; THYMUS SERPYLLUM; TRIBASIC CALCIUM PHOSPHATE

Active strength

8 [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

Pharmacologic classes

Blood Coagulation Factor [EPC], Calcium [CS], Calculi Dissolution Agent [EPC], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record