| Product NDC: | 37000-500 |
| Proprietary Name: | ZzzQuil |
| Non Proprietary Name: | DIPHENHYDRAMINE HYDROCHLORIDE |
| Active Ingredient(s): | 50 mg/30mL & nbsp; DIPHENHYDRAMINE HYDROCHLORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 37000-500 |
| Labeler Name: | Procter & Gamble Manufacruing Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part338 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20111208 |
| Package NDC: | 37000-500-06 |
| Package Description: | 177 mL in 1 BOTTLE, PLASTIC (37000-500-06) |
| NDC Code | 37000-500-06 |
| Proprietary Name | ZzzQuil |
| Package Description | 177 mL in 1 BOTTLE, PLASTIC (37000-500-06) |
| Product NDC | 37000-500 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | DIPHENHYDRAMINE HYDROCHLORIDE |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20111208 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Procter & Gamble Manufacruing Company |
| Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE |
| Strength Number | 50 |
| Strength Unit | mg/30mL |
| Pharmaceutical Classes |