| Product NDC: | 37808-906 | 
| Proprietary Name: | rx act cold and allergy | 
| Non Proprietary Name: | phenylephrine hcl, brompheniramine maleate | 
| Active Ingredient(s): | 1; 2.5 mg/5mL; mg/5mL & nbsp; phenylephrine hcl, brompheniramine maleate | 
| Administration Route(s): | ORAL | 
| Dosage Form(s): | LIQUID | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 37808-906 | 
| Labeler Name: | H E B | 
| Product Type: | HUMAN OTC DRUG | 
| FDA Application Number: | part341 | 
| Marketing Category: | OTC MONOGRAPH FINAL | 
| Start Marketing Date: | 20061016 | 
| Package NDC: | 37808-906-26 | 
| Package Description: | 1 BOTTLE in 1 CARTON (37808-906-26) > 118 mL in 1 BOTTLE | 
| NDC Code | 37808-906-26 | 
| Proprietary Name | rx act cold and allergy | 
| Package Description | 1 BOTTLE in 1 CARTON (37808-906-26) > 118 mL in 1 BOTTLE | 
| Product NDC | 37808-906 | 
| Product Type Name | HUMAN OTC DRUG | 
| Non Proprietary Name | phenylephrine hcl, brompheniramine maleate | 
| Dosage Form Name | LIQUID | 
| Route Name | ORAL | 
| Start Marketing Date | 20061016 | 
| Marketing Category Name | OTC MONOGRAPH FINAL | 
| Labeler Name | H E B | 
| Substance Name | BROMPHENIRAMINE MALEATE; PHENYLEPHRINE HYDROCHLORIDE | 
| Strength Number | 1; 2.5 | 
| Strength Unit | mg/5mL; mg/5mL | 
| Pharmaceutical Classes |