Radiation Protect

Product NDC
43742-0455
11-digit product format
437420455
Labeler code
43742
Product ID
43742-0455_bbc7e424-8db5-405f-81a0-c89edc9a8927
Type
HUMAN OTC DRUG
Nonproprietary name
Chondrus crispus, Fucus vesiculosus, Thyroidinum (suis), Cadmium iodatum, Cadmium sulphuratum, Iodium, Uranium nitricum, Radium bromatum,
Dosage form
LIQUID
Route
ORAL
Labeler
Deseret Biologicals, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2014-03-25
Marketing end
0000-00-00
Substance
CHONDRUS CRISPUS; FUCUS VESICULOSUS; SUS SCROFA THYROID; CADMIUM IODIDE; CADMIUM SULFIDE; IODINE; URANYL NITRATE HEXAHYDRATE; RADIUM BROMIDE; STRONTIUM CARBONATE; ALCOHOL, X-RAY EXPOSED (1000 RAD); ARNICA MONTANA
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_C]/mL
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
43742-0455-12023-12-11C16284748780-19d75b9d0-7bbe-f424-e053-dadaa90a57cee219db5e-e2b0-4482-9467-c88c39f53aa6
43742-0455-12020-01-31C16284748780-19d75b9d0-7bbe-f424-e053-dadaa90a57cee219db5e-e2b0-4482-9467-c88c39f53aa6