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Night Time Cough and Cold Relief
Night Time Cough and Cold Relief - 68016-137-00 - (DIPHENHYDRAMINE HYDROCHLORIDE, PHENYLEPHRINE HYDROCHLORIDE)
Drug Information of Night Time Cough and Cold Relief
| Product NDC: | 68016-137 |
| Proprietary Name: | Night Time Cough and Cold Relief |
| 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) |
Labeler Information of Night Time Cough and Cold Relief
| Product NDC: | 68016-137 |
| Labeler Name: | Chain Drug Consortium, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130101 |
Package Information of Night Time Cough and Cold Relief
| Package NDC: | 68016-137-00 |
| Package Description: | 120 mL in 1 BOTTLE (68016-137-00) |
NDC Information of Night Time Cough and Cold Relief
| NDC Code | 68016-137-00 |
| Proprietary Name | Night Time Cough and Cold Relief |
| Package Description | 120 mL in 1 BOTTLE (68016-137-00) |
| Product NDC | 68016-137 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | DIPHENHYDRAMINE HYDROCHLORIDE, PHENYLEPHRINE HYDROCHLORIDE |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20130101 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Chain Drug Consortium, LLC |
| Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 6.25; 2.5 |
| Strength Unit | mg/5mL; mg/5mL |
| Pharmaceutical Classes |
