| 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 |