Product NDC: | 43742-0240 |
Proprietary Name: | Radiation |
Non Proprietary Name: | Chondrus crispus, Fucus vesiculosus, Thyroidinum (suis), Cadmium iodatum, Iodium, Strontium carbonicum, X-Ray, |
Active Ingredient(s): | 30; 12; 3; 3; 12; 33; 12; 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 & nbsp; Chondrus crispus, Fucus vesiculosus, Thyroidinum (suis), Cadmium iodatum, Iodium, Strontium carbonicum, X-Ray, |
Administration Route(s): | ORAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 43742-0240 |
Labeler Name: | Deseret Biologicals, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 20121213 |
Package NDC: | 43742-0240-1 |
Package Description: | 30 mL in 1 BOTTLE, SPRAY (43742-0240-1) |
NDC Code | 43742-0240-1 |
Proprietary Name | Radiation |
Package Description | 30 mL in 1 BOTTLE, SPRAY (43742-0240-1) |
Product NDC | 43742-0240 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Chondrus crispus, Fucus vesiculosus, Thyroidinum (suis), Cadmium iodatum, Iodium, Strontium carbonicum, X-Ray, |
Dosage Form Name | LIQUID |
Route Name | ORAL |
Start Marketing Date | 20121213 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | Deseret Biologicals, Inc. |
Substance Name | ALCOHOL, X-RAY EXPOSED (1000 RAD); CADMIUM IODIDE; CHONDRUS CRISPUS; FUCUS VESICULOSUS; IODINE; RADIUM BROMIDE; STRONTIUM CARBONATE; THYROID, PORCINE |
Strength Number | 30; 12; 3; 3; 12; 33; 12; 8 |
Strength Unit | [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL |
Pharmaceutical Classes |