Label: RADIATION (chondrus crispus, fucus vesiculosus, thyroidinum- suis, cadmium iodatum, iodium, strontium carbonicum, x-ray, liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 43742-0240-1 - Packager: Deseret Biologicals, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved homeopathic
DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.
Drug Label Information
Updated December 13, 2012
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- ACTIVE INGREDIENTS:
- INDICATIONS:
- WARNINGS:
- DIRECTIONS:
- INACTIVE INGREDIENTS:
- KEEP OUT OF REACH OF CHILDREN.
- INDICATIONS:
- QUESTIONS:
- PACKAGE LABEL DISPLAY
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INGREDIENTS AND APPEARANCE
RADIATION
chondrus crispus, fucus vesiculosus, thyroidinum (suis), cadmium iodatum, iodium, strontium carbonicum, x-ray, liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:43742-0240 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CHONDRUS CRISPUS (UNII: OQS23HUA1X) (CHONDRUS CRISPUS - UNII:OQS23HUA1X) CHONDRUS CRISPUS 3 [hp_X] in 1 mL FUCUS VESICULOSUS (UNII: 535G2ABX9M) (FUCUS VESICULOSUS - UNII:535G2ABX9M) FUCUS VESICULOSUS 3 [hp_X] in 1 mL THYROID, PORCINE (UNII: 6RV024OAUQ) (SUS SCROFA THYROID - UNII:6RV024OAUQ) THYROID, PORCINE 8 [hp_X] in 1 mL CADMIUM IODIDE (UNII: 2F2UPU4KCW) (CADMIUM CATION - UNII:T494FZ4G8G) CADMIUM IODIDE 12 [hp_X] in 1 mL IODINE (UNII: 9679TC07X4) (IODINE - UNII:9679TC07X4) IODINE 12 [hp_X] in 1 mL STRONTIUM CARBONATE (UNII: 41YPU4MMCA) (STRONTIUM CATION - UNII:37077S2C93) STRONTIUM CARBONATE 12 [hp_X] in 1 mL ALCOHOL, X-RAY EXPOSED (1000 RAD) (UNII: 6PRJ93602P) (ALCOHOL, X-RAY EXPOSED (1000 RAD) - UNII:6PRJ93602P) ALCOHOL, X-RAY EXPOSED (1000 RAD) 30 [hp_X] in 1 mL RADIUM BROMIDE (UNII: R74O7T8569) (RADIUM CATION - UNII:05456MVL7T) RADIUM BROMIDE 33 [hp_X] in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALCOHOL (UNII: 3K9958V90M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:43742-0240-1 30 mL in 1 BOTTLE, SPRAY Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 12/13/2012 Labeler - Deseret Biologicals, Inc. (940741853) Registrant - Apotheca Company (844330915) Establishment Name Address ID/FEI Business Operations Apotheca Company 844330915 manufacture(43742-0240)