| Product NDC: | 37808-250 | 
| Proprietary Name: | cold relief | 
| Non Proprietary Name: | Acetaminophen, Chlorpheniramine maleate, Dextromethorphan HBr, Phenylephrine HCl | 
| Active Ingredient(s): | & nbsp; Acetaminophen, Chlorpheniramine maleate, Dextromethorphan HBr, Phenylephrine HCl | 
| Administration Route(s): | |
| Dosage Form(s): | KIT | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 37808-250 | 
| Labeler Name: | H E B | 
| Product Type: | HUMAN OTC DRUG | 
| FDA Application Number: | part341 | 
| Marketing Category: | OTC MONOGRAPH FINAL | 
| Start Marketing Date: | 20090211 | 
| Package NDC: | 37808-250-04 | 
| Package Description: | 1 KIT in 1 CARTON (37808-250-04) * 1 BLISTER PACK in 1 KIT > 12 TABLET, FILM COATED in 1 BLISTER PACK * 1 BLISTER PACK in 1 KIT > 12 TABLET, FILM COATED in 1 BLISTER PACK | 
| NDC Code | 37808-250-04 | 
| Proprietary Name | cold relief | 
| Package Description | 1 KIT in 1 CARTON (37808-250-04) * 1 BLISTER PACK in 1 KIT > 12 TABLET, FILM COATED in 1 BLISTER PACK * 1 BLISTER PACK in 1 KIT > 12 TABLET, FILM COATED in 1 BLISTER PACK | 
| Product NDC | 37808-250 | 
| Product Type Name | HUMAN OTC DRUG | 
| Non Proprietary Name | Acetaminophen, Chlorpheniramine maleate, Dextromethorphan HBr, Phenylephrine HCl | 
| Dosage Form Name | KIT | 
| Route Name | |
| Start Marketing Date | 20090211 | 
| Marketing Category Name | OTC MONOGRAPH FINAL | 
| Labeler Name | H E B | 
| Substance Name | |
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