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Day Time Cold Multi-Symptom Cool Blast
Day Time Cold Multi-Symptom Cool Blast - 49580-0192-8 - (Tylenol Multi Symptom Cool Blast Daytime)
Drug Information of Day Time Cold Multi-Symptom Cool Blast
| Product NDC: | 49580-0192 |
| Proprietary Name: | Day Time Cold Multi-Symptom Cool Blast |
| Non Proprietary Name: | Tylenol Multi Symptom Cool Blast Daytime |
| Active Ingredient(s): | 325; 10; 200; 5 mg/5mL; mg/5mL; mg/5mL; mg/5mL & nbsp; Tylenol Multi Symptom Cool Blast Daytime |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Day Time Cold Multi-Symptom Cool Blast
| Product NDC: | 49580-0192 |
| Labeler Name: | Aaron Industries, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100101 |
Package Information of Day Time Cold Multi-Symptom Cool Blast
| Package NDC: | 49580-0192-8 |
| Package Description: | 237 mL in 1 BOTTLE, PLASTIC (49580-0192-8) |
NDC Information of Day Time Cold Multi-Symptom Cool Blast
| NDC Code | 49580-0192-8 |
| Proprietary Name | Day Time Cold Multi-Symptom Cool Blast |
| Package Description | 237 mL in 1 BOTTLE, PLASTIC (49580-0192-8) |
| Product NDC | 49580-0192 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Tylenol Multi Symptom Cool Blast Daytime |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20100101 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Aaron Industries, Inc. |
| Substance Name | ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 325; 10; 200; 5 |
| Strength Unit | mg/5mL; mg/5mL; mg/5mL; mg/5mL |
| Pharmaceutical Classes |
