Product NDC: | 57520-0805 |
Proprietary Name: | Upper Respiratory Staph Strep Combo |
Non Proprietary Name: | Staphylococcus aureus, Klebsiella pneumoniae, Haemophilus influenzae, |
Active Ingredient(s): | 12; 15; 15 [hp_C]/mL; [hp_X]/mL; [hp_X]/mL & nbsp; Staphylococcus aureus, Klebsiella pneumoniae, Haemophilus influenzae, |
Administration Route(s): | ORAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 57520-0805 |
Labeler Name: | Apotheca Company |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 20110829 |
Package NDC: | 57520-0805-1 |
Package Description: | 30 mL in 1 BOTTLE, DROPPER (57520-0805-1) |
NDC Code | 57520-0805-1 |
Proprietary Name | Upper Respiratory Staph Strep Combo |
Package Description | 30 mL in 1 BOTTLE, DROPPER (57520-0805-1) |
Product NDC | 57520-0805 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Staphylococcus aureus, Klebsiella pneumoniae, Haemophilus influenzae, |
Dosage Form Name | LIQUID |
Route Name | ORAL |
Start Marketing Date | 20110829 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | Apotheca Company |
Substance Name | HAEMOPHILUS INFLUENZAE; KLEBSIELLA PNEUMONIAE; STAPHYLOCOCCUS AUREUS |
Strength Number | 12; 15; 15 |
Strength Unit | [hp_C]/mL; [hp_X]/mL; [hp_X]/mL |
Pharmaceutical Classes |