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ROBITUSSIN PEAK COLD NASAL RELIEF
ROBITUSSIN PEAK COLD NASAL RELIEF - 0031-8731-20 - (acetaminophen, phenylephrine HCl)
Drug Information of ROBITUSSIN PEAK COLD NASAL RELIEF
| Product NDC: | 0031-8731 |
| Proprietary Name: | ROBITUSSIN PEAK COLD NASAL RELIEF |
| Non Proprietary Name: | acetaminophen, phenylephrine HCl |
| Active Ingredient(s): | 325; 5 mg/1; mg/1 & nbsp; acetaminophen, phenylephrine HCl |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ROBITUSSIN PEAK COLD NASAL RELIEF
| Product NDC: | 0031-8731 |
| Labeler Name: | Richmond Division of Wyeth |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110606 |
Package Information of ROBITUSSIN PEAK COLD NASAL RELIEF
| Package NDC: | 0031-8731-20 |
| Package Description: | 2 BLISTER PACK in 1 CARTON (0031-8731-20) > 10 TABLET in 1 BLISTER PACK |
NDC Information of ROBITUSSIN PEAK COLD NASAL RELIEF
| NDC Code | 0031-8731-20 |
| Proprietary Name | ROBITUSSIN PEAK COLD NASAL RELIEF |
| Package Description | 2 BLISTER PACK in 1 CARTON (0031-8731-20) > 10 TABLET in 1 BLISTER PACK |
| Product NDC | 0031-8731 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | acetaminophen, phenylephrine HCl |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20110606 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Richmond Division of Wyeth |
| Substance Name | ACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 325; 5 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
