Home
>
National Drug Code (NDC)
>
Allergy Relief
Allergy Relief - 59726-720-05 - (Diphenhydramine HCl)
Drug Information of Allergy Relief
| Product NDC: | 59726-720 |
| 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) |
Labeler Information of Allergy Relief
| Product NDC: | 59726-720 |
| Labeler Name: | P and L Development of New York Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part336 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130207 |
Package Information of Allergy Relief
| Package NDC: | 59726-720-05 |
| Package Description: | 1 BLISTER PACK in 1 CARTON (59726-720-05) > 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK |
NDC Information of Allergy Relief
| NDC Code | 59726-720-05 |
| Proprietary Name | Allergy Relief |
| Package Description | 1 BLISTER PACK in 1 CARTON (59726-720-05) > 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK |
| Product NDC | 59726-720 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Diphenhydramine HCl |
| Dosage Form Name | CAPSULE, LIQUID FILLED |
| Route Name | ORAL |
| Start Marketing Date | 20130207 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | P and L Development of New York Corporation |
| Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE |
| Strength Number | 25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
