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Sinus Congestion and Pain Severe Daytime
Sinus Congestion and Pain Severe Daytime - 0363-5270-08 - (Aceetaminophen, Guaifenesin and Phenylephrine HCl)
Drug Information of Sinus Congestion and Pain Severe Daytime
| Product NDC: | 0363-5270 |
| Proprietary Name: | Sinus Congestion and Pain Severe Daytime |
| Non Proprietary Name: | Aceetaminophen, Guaifenesin and Phenylephrine HCl |
| Active Ingredient(s): | 325; 200; 5 mg/1; mg/1; mg/1 & nbsp; Aceetaminophen, Guaifenesin and Phenylephrine HCl |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sinus Congestion and Pain Severe Daytime
| Product NDC: | 0363-5270 |
| Labeler Name: | WALGREEN CO. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20050806 |
Package Information of Sinus Congestion and Pain Severe Daytime
| Package NDC: | 0363-5270-08 |
| Package Description: | 2 BLISTER PACK in 1 CARTON (0363-5270-08) > 12 TABLET in 1 BLISTER PACK |
NDC Information of Sinus Congestion and Pain Severe Daytime
| NDC Code | 0363-5270-08 |
| Proprietary Name | Sinus Congestion and Pain Severe Daytime |
| Package Description | 2 BLISTER PACK in 1 CARTON (0363-5270-08) > 12 TABLET in 1 BLISTER PACK |
| Product NDC | 0363-5270 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Aceetaminophen, Guaifenesin and Phenylephrine HCl |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20050806 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | WALGREEN CO. |
| Substance Name | ACETAMINOPHEN; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 325; 200; 5 |
| Strength Unit | mg/1; mg/1; mg/1 |
| Pharmaceutical Classes |
