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Intestaforce - 57520-0128-1 - (Intestaforce)

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Drug Information of Intestaforce

Product NDC: 57520-0128
Proprietary Name: Intestaforce
Non Proprietary Name: Intestaforce
Active Ingredient(s): 3; 3; 3; 3; 12; 12; 12; 12    [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;   Intestaforce
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Intestaforce

Product NDC: 57520-0128
Labeler Name: Apotheca Company
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20100323

Package Information of Intestaforce

Package NDC: 57520-0128-1
Package Description: 30 mL in 1 BOTTLE, DROPPER (57520-0128-1)

NDC Information of Intestaforce

NDC Code 57520-0128-1
Proprietary Name Intestaforce
Package Description 30 mL in 1 BOTTLE, DROPPER (57520-0128-1)
Product NDC 57520-0128
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Intestaforce
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20100323
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Apotheca Company
Substance Name ALTHAEA OFFICINALIS ROOT; CHILI PEPPER; COMFREY ROOT; FENNEL SEED; FERRUM PHOSPHORICUM; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; MERCURIUS SOLUBILIS; SILVER NITRATE
Strength Number 3; 3; 3; 3; 12; 12; 12; 12
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
Pharmaceutical Classes

Complete Information of Intestaforce


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