DeodoRite - 68703-007-80 - (Calc sulph, Carduus mar, Galium, Mag phos, Merc solub, Silicea, Acacia gum, lactose, magnesium stearate, starch, sucrose)

Alphabetical Index


Drug Information of DeodoRite

Product NDC: 68703-007
Proprietary Name: DeodoRite
Non Proprietary Name: Calc sulph, Carduus mar, Galium, Mag phos, Merc solub, Silicea, Acacia gum, lactose, magnesium stearate, starch, sucrose
Active Ingredient(s): 6; 3; 8; 30; 8; 3    [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_C]/1; [hp_X]/1; [hp_X]/1 & nbsp;   Calc sulph, Carduus mar, Galium, Mag phos, Merc solub, Silicea, Acacia gum, lactose, magnesium stearate, starch, sucrose
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of DeodoRite

Product NDC: 68703-007
Labeler Name: Native Remedies LLC
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20130102

Package Information of DeodoRite

Package NDC: 68703-007-80
Package Description: 180 TABLET in 1 BOTTLE, GLASS (68703-007-80)

NDC Information of DeodoRite

NDC Code 68703-007-80
Proprietary Name DeodoRite
Package Description 180 TABLET in 1 BOTTLE, GLASS (68703-007-80)
Product NDC 68703-007
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Calc sulph, Carduus mar, Galium, Mag phos, Merc solub, Silicea, Acacia gum, lactose, magnesium stearate, starch, sucrose
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130102
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Native Remedies LLC
Substance Name CALCIUM SULFATE ANHYDROUS; GALIUM APARINE; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; MERCURIUS SOLUBILIS; SILICON DIOXIDE; SILYBUM MARIANUM SEED
Strength Number 6; 3; 8; 30; 8; 3
Strength Unit [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_C]/1; [hp_X]/1; [hp_X]/1
Pharmaceutical Classes

Complete Information of DeodoRite


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