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ROBITUSSIN NIGHT TIME COUGH AND COLD
ROBITUSSIN NIGHT TIME COUGH AND COLD - 0031-8698-13 - (diphenhydramine HCl, phenylephrine HCl)
Drug Information of ROBITUSSIN NIGHT TIME COUGH AND COLD
| Product NDC: | 0031-8698 |
| Proprietary Name: | ROBITUSSIN NIGHT TIME COUGH AND COLD |
| Non Proprietary Name: | diphenhydramine HCl, phenylephrine HCl |
| Active Ingredient(s): | 6.25; 2.5 mg/5mL; mg/5mL & nbsp; diphenhydramine HCl, phenylephrine HCl |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ROBITUSSIN NIGHT TIME COUGH AND COLD
| Product NDC: | 0031-8698 |
| Labeler Name: | Richmond Division of Wyeth |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20060209 |
Package Information of ROBITUSSIN NIGHT TIME COUGH AND COLD
| Package NDC: | 0031-8698-13 |
| Package Description: | 1 BOTTLE in 1 CARTON (0031-8698-13) > 118 mL in 1 BOTTLE |
NDC Information of ROBITUSSIN NIGHT TIME COUGH AND COLD
| NDC Code | 0031-8698-13 |
| Proprietary Name | ROBITUSSIN NIGHT TIME COUGH AND COLD |
| Package Description | 1 BOTTLE in 1 CARTON (0031-8698-13) > 118 mL in 1 BOTTLE |
| Product NDC | 0031-8698 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | diphenhydramine HCl, phenylephrine HCl |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20060209 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Richmond Division of Wyeth |
| Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 6.25; 2.5 |
| Strength Unit | mg/5mL; mg/5mL |
| Pharmaceutical Classes |
