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Inflammation I - 57520-0148-1 - (Inflammation I)

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Drug Information of Inflammation I

Product NDC: 57520-0148
Proprietary Name: Inflammation I
Non Proprietary Name: Inflammation I
Active Ingredient(s): 12; 12; 3; 12; 3; 12; 12; 3; 3; 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; [hp_X]/mL; [hp_X]/mL & nbsp;   Inflammation I
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Inflammation I

Product NDC: 57520-0148
Labeler Name: Apotheca Company
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20100309

Package Information of Inflammation I

Package NDC: 57520-0148-1
Package Description: 30 mL in 1 BOTTLE, DROPPER (57520-0148-1)

NDC Information of Inflammation I

NDC Code 57520-0148-1
Proprietary Name Inflammation I
Package Description 30 mL in 1 BOTTLE, DROPPER (57520-0148-1)
Product NDC 57520-0148
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Inflammation I
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20100309
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Apotheca Company
Substance Name APIS MELLIFERA; ATROPA BELLADONNA; ECHINACEA ANGUSTIFOLIA; FERRUM PHOSPHORICUM; GOLDENSEAL; NERIUM OLEANDER LEAF; NITRIC ACID; PHYTOLACCA AMERICANA ROOT; RORIPPA NASTURTIUM-AQUATICUM; SILICON DIOXIDE
Strength Number 12; 12; 3; 12; 3; 12; 12; 3; 3; 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; [hp_X]/mL; [hp_X]/mL
Pharmaceutical Classes

Complete Information of Inflammation I


General Information