| Product NDC: | 47682-307 |
| Proprietary Name: | Dover Coldonyl |
| Non Proprietary Name: | ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE |
| Active Ingredient(s): | 325; 100; 5 mg/1; mg/1; mg/1 & nbsp; ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 47682-307 |
| Labeler Name: | Unifirst First Aid Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20081230 |
| Package NDC: | 47682-307-13 |
| Package Description: | 250 PACKET in 1 BOX, UNIT-DOSE (47682-307-13) > 2 TABLET in 1 PACKET (47682-307-99) |
| NDC Code | 47682-307-13 |
| Proprietary Name | Dover Coldonyl |
| Package Description | 250 PACKET in 1 BOX, UNIT-DOSE (47682-307-13) > 2 TABLET in 1 PACKET (47682-307-99) |
| Product NDC | 47682-307 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20081230 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Unifirst First Aid Corporation |
| Substance Name | ACETAMINOPHEN; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 325; 100; 5 |
| Strength Unit | mg/1; mg/1; mg/1 |
| Pharmaceutical Classes |