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MULTI-SYMPTOM ALLERGY
MULTI-SYMPTOM ALLERGY - 62011-0056-1 - (diphenhydramine hydrochloride)
Drug Information of MULTI-SYMPTOM ALLERGY
| Product NDC: | 62011-0056 |
| Proprietary Name: | MULTI-SYMPTOM ALLERGY |
| Non Proprietary Name: | diphenhydramine hydrochloride |
| Active Ingredient(s): | 25 mg/1 & nbsp; diphenhydramine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of MULTI-SYMPTOM ALLERGY
| Product NDC: | 62011-0056 |
| Labeler Name: | McKesson (Health Mart) |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120214 |
Package Information of MULTI-SYMPTOM ALLERGY
| Package NDC: | 62011-0056-1 |
| Package Description: | 24 CAPSULE in 1 BOTTLE (62011-0056-1) |
NDC Information of MULTI-SYMPTOM ALLERGY
| NDC Code | 62011-0056-1 |
| Proprietary Name | MULTI-SYMPTOM ALLERGY |
| Package Description | 24 CAPSULE in 1 BOTTLE (62011-0056-1) |
| Product NDC | 62011-0056 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | diphenhydramine hydrochloride |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20120214 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | McKesson (Health Mart) |
| Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE |
| Strength Number | 25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
