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Rx Act sinus and allergy PE
Rx Act sinus and allergy PE - 37808-358-62 - (Chlorpheniramine maleate, Phenylephrine HCl)
Drug Information of Rx Act sinus and allergy PE
| Product NDC: | 37808-358 |
| Proprietary Name: | Rx Act sinus and allergy PE |
| Non Proprietary Name: | Chlorpheniramine maleate, Phenylephrine HCl |
| Active Ingredient(s): | 4; 10 mg/1; mg/1 & nbsp; Chlorpheniramine maleate, Phenylephrine HCl |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Rx Act sinus and allergy PE
| Product NDC: | 37808-358 |
| Labeler Name: | H E B |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100521 |
Package Information of Rx Act sinus and allergy PE
| Package NDC: | 37808-358-62 |
| Package Description: | 1 BLISTER PACK in 1 CARTON (37808-358-62) > 24 TABLET, FILM COATED in 1 BLISTER PACK |
NDC Information of Rx Act sinus and allergy PE
| NDC Code | 37808-358-62 |
| Proprietary Name | Rx Act sinus and allergy PE |
| Package Description | 1 BLISTER PACK in 1 CARTON (37808-358-62) > 24 TABLET, FILM COATED in 1 BLISTER PACK |
| Product NDC | 37808-358 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Chlorpheniramine maleate, Phenylephrine HCl |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20100521 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | H E B |
| Substance Name | CHLORPHENIRAMINE MALEATE; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 4; 10 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
