Product NDC: | 49580-2004 |
Proprietary Name: | Flu Relief Therapy Night Time |
Non Proprietary Name: | Acetaminophen, DIPHENHYDRAMINE HYDROCHLORIDE, Phenylephrine Hydrochloride |
Active Ingredient(s): | 325; 12.5; 5 mg/15mL; mg/15mL; mg/15mL & nbsp; Acetaminophen, DIPHENHYDRAMINE HYDROCHLORIDE, Phenylephrine Hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49580-2004 |
Labeler Name: | Aaron Industries, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20091001 |
Package NDC: | 49580-2004-8 |
Package Description: | 245 mL in 1 BOTTLE, PLASTIC (49580-2004-8) |
NDC Code | 49580-2004-8 |
Proprietary Name | Flu Relief Therapy Night Time |
Package Description | 245 mL in 1 BOTTLE, PLASTIC (49580-2004-8) |
Product NDC | 49580-2004 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Acetaminophen, DIPHENHYDRAMINE HYDROCHLORIDE, Phenylephrine Hydrochloride |
Dosage Form Name | LIQUID |
Route Name | ORAL |
Start Marketing Date | 20091001 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Aaron Industries, Inc. |
Substance Name | ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE; PHENYLEPHRINE HYDROCHLORIDE |
Strength Number | 325; 12.5; 5 |
Strength Unit | mg/15mL; mg/15mL; mg/15mL |
Pharmaceutical Classes |