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Candicide 12X - 62713-925-01 - (Candicide 12X)

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Drug Information of Candicide 12X

Product NDC: 62713-925
Proprietary Name: Candicide 12X
Non Proprietary Name: Candicide 12X
Active Ingredient(s): 3; 12; 30; 30; 30; 30; 30; 30; 30; 30    [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 & nbsp;   Candicide 12X
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Candicide 12X

Product NDC: 62713-925
Labeler Name: Meditrend, Inc. DBA Progena Professional Formulations
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 19840301

Package Information of Candicide 12X

Package NDC: 62713-925-01
Package Description: 30 mL in 1 BOTTLE, DROPPER (62713-925-01)

NDC Information of Candicide 12X

NDC Code 62713-925-01
Proprietary Name Candicide 12X
Package Description 30 mL in 1 BOTTLE, DROPPER (62713-925-01)
Product NDC 62713-925
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Candicide 12X
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 19840301
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Meditrend, Inc. DBA Progena Professional Formulations
Substance Name BAPTISIA TINCTORIA ROOT; CANDIDA ALBICANS; LYCOPODIUM CLAVATUM SPORE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; PHOSPHORIC ACID; PULSATILLA VULGARIS; SEPIA OFFICINALIS JUICE; SODIUM BORATE; STRYCHNOS NUX-VOMICA SEED; WOOD CREOSOTE
Strength Number 3; 12; 30; 30; 30; 30; 30; 30; 30; 30
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; [hp_X]/mL; [hp_X]/mL
Pharmaceutical Classes

Complete Information of Candicide 12X


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