Product NDC: | 49523-505 |
Proprietary Name: | Baczol Cold Medicine |
Non Proprietary Name: | ACETAMINOPHEN, PHENYLEPHRINE HYDROCHLORIDE, DEXTROMETHORPHAN HYDROBROMIDE, and CHLORPHENIRAMINE MALEATE |
Active Ingredient(s): | 250; 4; 10; 10 mg/5mL; mg/5mL; mg/5mL; mg/5mL & nbsp; ACETAMINOPHEN, PHENYLEPHRINE HYDROCHLORIDE, DEXTROMETHORPHAN HYDROBROMIDE, and CHLORPHENIRAMINE MALEATE |
Administration Route(s): | ORAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49523-505 |
Labeler Name: | Lex Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20130204 |
Package NDC: | 49523-505-04 |
Package Description: | 1 BOTTLE in 1 CARTON (49523-505-04) > 120 mL in 1 BOTTLE |
NDC Code | 49523-505-04 |
Proprietary Name | Baczol Cold Medicine |
Package Description | 1 BOTTLE in 1 CARTON (49523-505-04) > 120 mL in 1 BOTTLE |
Product NDC | 49523-505 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | ACETAMINOPHEN, PHENYLEPHRINE HYDROCHLORIDE, DEXTROMETHORPHAN HYDROBROMIDE, and CHLORPHENIRAMINE MALEATE |
Dosage Form Name | LIQUID |
Route Name | ORAL |
Start Marketing Date | 20130204 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Lex Inc |
Substance Name | ACETAMINOPHEN; CHLORPHENIRAMINE MALEATE; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE |
Strength Number | 250; 4; 10; 10 |
Strength Unit | mg/5mL; mg/5mL; mg/5mL; mg/5mL |
Pharmaceutical Classes |