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Robitussin Peak Cold Multi-Symptom Cold
Robitussin Peak Cold Multi-Symptom Cold - 0031-8742-14 - (dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride)
Drug Information of Robitussin Peak Cold Multi-Symptom Cold
| Product NDC: | 0031-8742 |
| Proprietary Name: | Robitussin Peak Cold Multi-Symptom Cold |
| Non Proprietary Name: | dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride |
| Active Ingredient(s): | 10; 100; 5 mg/5mL; mg/5mL; mg/5mL & nbsp; dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Robitussin Peak Cold Multi-Symptom Cold
| Product NDC: | 0031-8742 |
| Labeler Name: | Richmond Division of Wyeth |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110612 |
Package Information of Robitussin Peak Cold Multi-Symptom Cold
| Package NDC: | 0031-8742-14 |
| Package Description: | 1 BOTTLE in 1 CARTON (0031-8742-14) > 118 mL in 1 BOTTLE |
NDC Information of Robitussin Peak Cold Multi-Symptom Cold
| NDC Code | 0031-8742-14 |
| Proprietary Name | Robitussin Peak Cold Multi-Symptom Cold |
| Package Description | 1 BOTTLE in 1 CARTON (0031-8742-14) > 118 mL in 1 BOTTLE |
| Product NDC | 0031-8742 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20110612 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Richmond Division of Wyeth |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 10; 100; 5 |
| Strength Unit | mg/5mL; mg/5mL; mg/5mL |
| Pharmaceutical Classes |
