Product NDC: | 24286-1546 |
Proprietary Name: | Bactimicina Cough and Cold |
Non Proprietary Name: | DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE |
Active Ingredient(s): | 10; 100; 5 mg/5mL; mg/5mL; mg/5mL & nbsp; DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE |
Administration Route(s): | ORAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 24286-1546 |
Labeler Name: | DLC Laboratories, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20110606 |
Package NDC: | 24286-1546-4 |
Package Description: | 1 BOTTLE in 1 BOX (24286-1546-4) > 118 mL in 1 BOTTLE |
NDC Code | 24286-1546-4 |
Proprietary Name | Bactimicina Cough and Cold |
Package Description | 1 BOTTLE in 1 BOX (24286-1546-4) > 118 mL in 1 BOTTLE |
Product NDC | 24286-1546 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE |
Dosage Form Name | LIQUID |
Route Name | ORAL |
Start Marketing Date | 20110606 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | DLC Laboratories, Inc. |
Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
Strength Number | 10; 100; 5 |
Strength Unit | mg/5mL; mg/5mL; mg/5mL |
Pharmaceutical Classes |