Product NDC: | 35418-111 |
Proprietary Name: | Histenol Forte II |
Non Proprietary Name: | Phenylephrine HCl, Acetaminophen, Guaifenesin |
Active Ingredient(s): | 325; 100; 5 mg/1; mg/1; mg/1 & nbsp; Phenylephrine HCl, Acetaminophen, Guaifenesin |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 35418-111 |
Labeler Name: | Zee Medical Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20120612 |
Package NDC: | 35418-111-67 |
Package Description: | 125 CARTON in 1 CARTON (35418-111-67) > 50 PACKET in 1 CARTON (35418-111-68) > 2 TABLET in 1 PACKET (35418-111-02) |
NDC Code | 35418-111-67 |
Proprietary Name | Histenol Forte II |
Package Description | 125 CARTON in 1 CARTON (35418-111-67) > 50 PACKET in 1 CARTON (35418-111-68) > 2 TABLET in 1 PACKET (35418-111-02) |
Product NDC | 35418-111 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Phenylephrine HCl, Acetaminophen, Guaifenesin |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20120612 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Zee Medical Inc |
Substance Name | ACETAMINOPHEN; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
Strength Number | 325; 100; 5 |
Strength Unit | mg/1; mg/1; mg/1 |
Pharmaceutical Classes |