Product NDC: | 50804-720 |
Proprietary Name: | Allergy Relief |
Non Proprietary Name: | Diphenhydramine HCl |
Active Ingredient(s): | 25 mg/1 & nbsp; Diphenhydramine HCl |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE, LIQUID FILLED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 50804-720 |
Labeler Name: | Good Sense (Geiss, Destin & Dunn, Inc.) |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part336 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20130606 |
Package NDC: | 50804-720-24 |
Package Description: | 2 BLISTER PACK in 1 CARTON (50804-720-24) > 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK |
NDC Code | 50804-720-24 |
Proprietary Name | Allergy Relief |
Package Description | 2 BLISTER PACK in 1 CARTON (50804-720-24) > 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK |
Product NDC | 50804-720 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Diphenhydramine HCl |
Dosage Form Name | CAPSULE, LIQUID FILLED |
Route Name | ORAL |
Start Marketing Date | 20130606 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Good Sense (Geiss, Destin & Dunn, Inc.) |
Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE |
Strength Number | 25 |
Strength Unit | mg/1 |
Pharmaceutical Classes |