| NDC Code: |
49580-0192 |
| Proprietary Name: |
Day Time Cold Multi-Symptom Cool Blast |
| Suffix: |
|
| Non-Proprietary Name: |
Tylenol Multi Symptom Cool Blast Daytime |
| Dosage Form: |
LIQUID |
| Method: |
ORAL |
| Original Marketing Date: |
01-01-2010 |
| Category Name: |
OTC MONOGRAPH FINAL |
| Application Number: |
part341 |
| Labeler: |
AARON INDUSTRIES, INC. |
| Substance Name: |
ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
| Active Numerator Strength: |
325; 10; 200; 5 |
| Active Ingredient Unit: |
mg/5mL; mg/5mL; mg/5mL; mg/5mL |
| Pharm Classes: |
|
| DEA Schedule: |
|
