EMF Protect and Balance

Product NDC
43742-0453
11-digit product format
437420453
Labeler code
43742
Product ID
43742-0453_e70e3c4b-36c7-4972-84f3-487cf6480079
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
2014-03-18
Marketing end
2020-08-05
Substance
ALFALFA; LAMINARIA DIGITATA; COMFREY ROOT; ASCORBIC ACID; MELATONIN; OYSTER SHELL CALCIUM CARBONATE, CRUDE; COPPER; IRON; IODINE; MANGANESE ACETATE TETRAHYDRATE; SILICON DIOXIDE; PHOSPHORUS; ALCOHOL, X-RAY EXPOSED (1000 RAD); 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