| Product NDC: | 21130-152 |
| Proprietary Name: | Triacting Night Time |
| Non Proprietary Name: | DIPHENHYDRAMINE HYDROCHLORIDE, PHENYLEPHRINE HYDROCHLORIDE |
| Active Ingredient(s): | 6.25; 2.5 mg/5mL; mg/5mL & nbsp; DIPHENHYDRAMINE HYDROCHLORIDE, PHENYLEPHRINE HYDROCHLORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 21130-152 |
| Labeler Name: | Safeway |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20090323 |
| Package NDC: | 21130-152-04 |
| Package Description: | 118 mL in 1 BOTTLE, PLASTIC (21130-152-04) |
| NDC Code | 21130-152-04 |
| Proprietary Name | Triacting Night Time |
| Package Description | 118 mL in 1 BOTTLE, PLASTIC (21130-152-04) |
| Product NDC | 21130-152 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | DIPHENHYDRAMINE HYDROCHLORIDE, PHENYLEPHRINE HYDROCHLORIDE |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20090323 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Safeway |
| Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 6.25; 2.5 |
| Strength Unit | mg/5mL; mg/5mL |
| Pharmaceutical Classes |