Product NDC: | 62750-022 |
Proprietary Name: | Zicam |
Non Proprietary Name: | acetaminophen, dextromethorphan hydrobromide and guaifenesin |
Active Ingredient(s): | 325; 10; 200 mg/15mL; mg/15mL; mg/15mL & nbsp; acetaminophen, dextromethorphan hydrobromide and guaifenesin |
Administration Route(s): | ORAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 62750-022 |
Labeler Name: | Matrixx Initiatives, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20070716 |
Package NDC: | 62750-022-10 |
Package Description: | 240 mL in 1 BOTTLE, UNIT-DOSE (62750-022-10) |
NDC Code | 62750-022-10 |
Proprietary Name | Zicam |
Package Description | 240 mL in 1 BOTTLE, UNIT-DOSE (62750-022-10) |
Product NDC | 62750-022 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | acetaminophen, dextromethorphan hydrobromide and guaifenesin |
Dosage Form Name | LIQUID |
Route Name | ORAL |
Start Marketing Date | 20070716 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Matrixx Initiatives, Inc. |
Substance Name | ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN |
Strength Number | 325; 10; 200 |
Strength Unit | mg/15mL; mg/15mL; mg/15mL |
Pharmaceutical Classes |