Universaltox

Product NDC

43857-0246

11-digit product format

438570246

Labeler code

43857

Product ID

43857-0246_e2996297-9e23-4d3b-85a3-3d9f9fb6e65f

Type

HUMAN OTC DRUG

Nonproprietary name

Alfalfa, Avena Sativa, Fucus Vesiculosus, Hordeum Vulgare, Nasturtium Aquaticum, Raphanus Sativus, Triticum Aestivum, Iodium, Ubiquinone

Dosage form

LIQUID

Route

ORAL

Labeler

BioActive Nutritional, Inc.

Marketing category

UNAPPROVED HOMEOPATHIC

Marketing start

2014-01-10

Marketing end

2022-06-20

Substance

ALFALFA; AVENA SATIVA FLOWERING TOP; FUCUS VESICULOSUS; HORDEUM VULGARE TOP; NASTURTIUM OFFICINALE; RAPHANUS SATIVUS; TRITICUM AESTIVUM WHOLE; IODINE; UBIDECARENONE; SUS SCROFA ADRENAL GLAND; PORK LIVER; MANGANESE GLUCONATE; BROWN RICE; SUS SCROFA THYROID; OYSTER SHELL CALCIUM CARBONATE, CRUDE; SODIUM CHLORIDE; PULSATILLA VULGARIS; TOXICODENDRON PUBESCENS LEAF; CORTISONE ACETATE; PARAFFIN; ETHYLENE GLYCOL; PROPYL ALCOHOL; PALMITIC ACID; DIMETHICONE; POLYACRYLIC ACID (8000 MW); GLUTARAL; METHYL ACRYLATE; ANHYDROUS CITRIC ACID; TARTARIC ACID; ANTHRAQUINONE; HYDROGEN PEROXIDE; GLYCOLIC ACID; AMMONIUM THIOGLYCOLATE; SODIUM CARBONATE; MONOETHANOLAMINE; TOLUENE-2,5-DIAMINE; P-AMINOPHENOL

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; [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