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Severe Cold Relief PE
Severe Cold Relief PE - 59779-652-07 - (Acetaminophen, Diphenhydramine HCl and Phenylephrine HCl)
Drug Information of Severe Cold Relief PE
| Product NDC: | 59779-652 |
| Proprietary Name: | Severe Cold Relief PE |
| Non Proprietary Name: | Acetaminophen, Diphenhydramine HCl and Phenylephrine HCl |
| Active Ingredient(s): | 325; 12.5; 5 mg/1; mg/1; mg/1 & nbsp; Acetaminophen, Diphenhydramine HCl and Phenylephrine HCl |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Severe Cold Relief PE
| Product NDC: | 59779-652 |
| Labeler Name: | WOONSOCKET PRESCRIPTION CENTER,INCORPORATED |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20050621 |
Package Information of Severe Cold Relief PE
| Package NDC: | 59779-652-07 |
| Package Description: | 1 BLISTER PACK in 1 CARTON (59779-652-07) > 36 TABLET, FILM COATED in 1 BLISTER PACK |
NDC Information of Severe Cold Relief PE
| NDC Code | 59779-652-07 |
| Proprietary Name | Severe Cold Relief PE |
| Package Description | 1 BLISTER PACK in 1 CARTON (59779-652-07) > 36 TABLET, FILM COATED in 1 BLISTER PACK |
| Product NDC | 59779-652 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen, Diphenhydramine HCl and Phenylephrine HCl |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20050621 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | WOONSOCKET PRESCRIPTION CENTER,INCORPORATED |
| Substance Name | ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 325; 12.5; 5 |
| Strength Unit | mg/1; mg/1; mg/1 |
| Pharmaceutical Classes |
