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Unisom SleepMelts
Unisom SleepMelts - 41167-0014-0 - (Diphenhydramine Hydrochloride)
Drug Information of Unisom SleepMelts
| Product NDC: | 41167-0014 |
| Proprietary Name: | Unisom SleepMelts |
| Non Proprietary Name: | Diphenhydramine Hydrochloride |
| Active Ingredient(s): | 25 mg/1 & nbsp; Diphenhydramine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, CHEWABLE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Unisom SleepMelts
| Product NDC: | 41167-0014 |
| Labeler Name: | Chattem, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part338 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20080101 |
Package Information of Unisom SleepMelts
| Package NDC: | 41167-0014-0 |
| Package Description: | 3 BLISTER PACK in 1 CARTON (41167-0014-0) > 8 TABLET, CHEWABLE in 1 BLISTER PACK |
NDC Information of Unisom SleepMelts
| NDC Code | 41167-0014-0 |
| Proprietary Name | Unisom SleepMelts |
| Package Description | 3 BLISTER PACK in 1 CARTON (41167-0014-0) > 8 TABLET, CHEWABLE in 1 BLISTER PACK |
| Product NDC | 41167-0014 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Diphenhydramine Hydrochloride |
| Dosage Form Name | TABLET, CHEWABLE |
| Route Name | ORAL |
| Start Marketing Date | 20080101 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Chattem, Inc. |
| Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE |
| Strength Number | 25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
