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NDC 43742-2080-01 Radiation Plus 30; 30; 12; 12; 3; 12; 12; 12; 12; 12; 8; 12 [hp_X]/mL; [hp_C]/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 Details
Radiation Plus 30; 30; 12; 12; 3; 12; 12; 12; 12; 12; 8; 12 [hp_X]/mL; [hp_C]/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
Radiation Plus is a ORAL LIQUID in the HUMAN OTC DRUG category. It is labeled and distributed by Deseret Biologicals, Inc.. The primary component is ALCOHOL, X-RAY EXPOSED (1000 RAD); ARNICA MONTANA WHOLE; CADMIUM SULFIDE; COLCHICUM AUTUMNALE BULB; FUCUS VESICULOSUS; HERRING SPERM DNA; IODINE; LEAD; RADIUM BROMIDE; STRONTIUM CARBONATE; THYROID, PORCINE; VISCUM ALBUM FRUITING TOP.
Product Information
| NDC | 43742-2080 |
|---|---|
| Product ID | 43742-2080_357a8667-22a8-4c7f-8e34-a897f3dac3b4 |
| Associated GPIs | |
| GCN Sequence Number | n/a |
| GCN Sequence Number Description | n/a |
| HIC3 | n/a |
| HIC3 Description | n/a |
| GCN | n/a |
| HICL Sequence Number | n/a |
| HICL Sequence Number Description | n/a |
| Brand/Generic | n/a |
| Proprietary Name | Radiation Plus |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Fucus Vesiculosus, Thyroidinum (Suis), Cadmium Sulphuratum, Colchicum Autumnale, DNA, Iodium, Plumbum Metallicum, Radium Bromatum, Strontium Carbonicum, Viscum Album, X-Ray, Arnica Montana |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | LIQUID |
| Route | ORAL |
| Active Ingredient Strength | 30; 30; 12; 12; 3; 12; 12; 12; 12; 12; 8; 12 |
| Active Ingredient Units | [hp_X]/mL; [hp_C]/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 |
| Substance Name | ALCOHOL, X-RAY EXPOSED (1000 RAD); ARNICA MONTANA WHOLE; CADMIUM SULFIDE; COLCHICUM AUTUMNALE BULB; FUCUS VESICULOSUS; HERRING SPERM DNA; IODINE; LEAD; RADIUM BROMIDE; STRONTIUM CARBONATE; THYROID, PORCINE; VISCUM ALBUM FRUITING TOP |
| Labeler Name | Deseret Biologicals, Inc. |
| Pharmaceutical Class | n/a |
| DEA Schedule | n/a |
| Marketing Category | UNAPPROVED HOMEOPATHIC |
| Application Number | n/a |
| Listing Certified Through | 2024-12-31 |
Package
NDC 43742-2080-01 (43742208001)
| NDC Package Code | 43742-2080-1 |
|---|---|
| Billing NDC | 43742208001 |
| Package | 30 mL in 1 BOTTLE, DROPPER (43742-2080-1) |
| Marketing Start Date | 2023-04-11 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |