Product NDC: | 49580-1434 |
Proprietary Name: | Childrens Plus Multi-Symptom Cold Grape |
Non Proprietary Name: | Childrens Tylenol Plus Multi-Symptom Cold |
Active Ingredient(s): | 160; 1; 5; 2.5 mg/5mL; mg/5mL; mg/5mL; mg/5mL & nbsp; Childrens Tylenol Plus Multi-Symptom Cold |
Administration Route(s): | ORAL |
Dosage Form(s): | SUSPENSION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49580-1434 |
Labeler Name: | Aaron Industries, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20090101 |
Package NDC: | 49580-1434-4 |
Package Description: | 118 mL in 1 BOTTLE, PLASTIC (49580-1434-4) |
NDC Code | 49580-1434-4 |
Proprietary Name | Childrens Plus Multi-Symptom Cold Grape |
Package Description | 118 mL in 1 BOTTLE, PLASTIC (49580-1434-4) |
Product NDC | 49580-1434 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Childrens Tylenol Plus Multi-Symptom Cold |
Dosage Form Name | SUSPENSION |
Route Name | ORAL |
Start Marketing Date | 20090101 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Aaron Industries, Inc. |
Substance Name | ACETAMINOPHEN; CHLORPHENIRAMINE MALEATE; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE |
Strength Number | 160; 1; 5; 2.5 |
Strength Unit | mg/5mL; mg/5mL; mg/5mL; mg/5mL |
Pharmaceutical Classes |