EMF Protect and Balance

Product NDC

43742-0673

11-digit product format

437420673

Labeler code

43742

Product ID

43742-0673_279b3144-84f0-4f53-94f0-80ea0af19df9

Type

HUMAN OTC DRUG

Nonproprietary name

Alfalfa, Laminaria Digitata, Symphytum Officinale, Ascorbic Acid, Melatonin, Calcarea Carbonica, Cuprum Metallicum, Ferrum Metallicum, Iodium, Manganum Aceticum, Silicea, Phosphorus, Magnetis Polus Arcticus, Magnetis Polus Australis, X-Ray, Agate, Quartz, Carbon Dioxide, Aconitum Napellus, Arsenicum Album, Gaertner Bacillus (Bach), Kali Carbonicum

Dosage form

LIQUID

Route

ORAL

Labeler

Deseret Biologicals, Inc.

Marketing category

UNAPPROVED HOMEOPATHIC

Marketing start

2015-11-20

Marketing end

2021-12-23

Substance

ALFALFA; LAMINARIA DIGITATA; COMFREY ROOT; ASCORBIC ACID; MELATONIN; OYSTER SHELL CALCIUM CARBONATE, CRUDE; COPPER; IRON; IODINE; MANGANESE ACETATE TETRAHYDRATE; PHOSPHORUS; ALCOHOL, X-RAY EXPOSED (1000 RAD); SILICON DIOXIDE; CARBON DIOXIDE; ACONITUM NAPELLUS; ARSENIC TRIOXIDE; SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS; POTASSIUM CARBONATE

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_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record