| 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 |