| Product NDC: | 37808-476 | 
| Proprietary Name: | Allergy | 
| Non Proprietary Name: | Acetaminophen, Chlorpheniramine maleate, Phenylephrine HCl | 
| Active Ingredient(s): | 325; 2; 5 mg/1; mg/1; mg/1 & nbsp; Acetaminophen, Chlorpheniramine maleate, Phenylephrine HCl | 
| Administration Route(s): | ORAL | 
| Dosage Form(s): | TABLET | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 37808-476 | 
| Labeler Name: | H E B | 
| Product Type: | HUMAN OTC DRUG | 
| FDA Application Number: | part341 | 
| Marketing Category: | OTC MONOGRAPH FINAL | 
| Start Marketing Date: | 20060117 | 
| Package NDC: | 37808-476-62 | 
| Package Description: | 2 BLISTER PACK in 1 CARTON (37808-476-62) > 12 TABLET in 1 BLISTER PACK | 
| NDC Code | 37808-476-62 | 
| Proprietary Name | Allergy | 
| Package Description | 2 BLISTER PACK in 1 CARTON (37808-476-62) > 12 TABLET in 1 BLISTER PACK | 
| Product NDC | 37808-476 | 
| Product Type Name | HUMAN OTC DRUG | 
| Non Proprietary Name | Acetaminophen, Chlorpheniramine maleate, Phenylephrine HCl | 
| Dosage Form Name | TABLET | 
| Route Name | ORAL | 
| Start Marketing Date | 20060117 | 
| Marketing Category Name | OTC MONOGRAPH FINAL | 
| Labeler Name | H E B | 
| Substance Name | ACETAMINOPHEN; CHLORPHENIRAMINE MALEATE; PHENYLEPHRINE HYDROCHLORIDE | 
| Strength Number | 325; 2; 5 | 
| Strength Unit | mg/1; mg/1; mg/1 | 
| Pharmaceutical Classes |