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Robitussin Peak Cold Multi-Symptom Cold - 0031-8742-14 - (dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride)

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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

Complete Information of Robitussin Peak Cold Multi-Symptom Cold


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