0031-8742 : Robitussin Peak Cold Multi-symptom Cold Oral Liquid


NDC: 0031-8742
Labeler: Richmond Division of Wyeth
Product Type: Human OTC Drug
Drug Name:  Robitussin Peak Cold Multi-symptom Cold
Dosage Form: Oral Liquid
Application #: part341
Rev. Date: 


NDC Package Codes:

  • 0031-8742-14: 1 BOTTLE IN 1 CARTON (0031‑8742‑14) > 118 ML IN 1 BOTTLE
  • 0031-8742-20: 1 BOTTLE IN 1 CARTON (0031‑8742‑20) > 237 ML IN 1 BOTTLE

Active Ingredients:

  • Dextromethorphan Hydrobromide
  • Guaifenesin
  • Phenylephrine Hydrochloride

Dosage Strength:

  • 10 mg/5mL
  • 100 mg/5mL
  • 5 mg/5mL

Pharmaceutical Classes:

  • Adrenergic alpha1-Agonists [MoA]
  • Decreased Respiratory Secretion Viscosity [PE]
  • Expectorant [EPC]
  • Increased Respiratory Secretions [PE]
  • Sigma-1 Agonist [EPC]
  • Sigma-1 Receptor Agonists [MoA]
  • Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC]
  • Uncompetitive NMDA Receptor Antagonists [MoA]
  • alpha-1 Adrenergic Agonist [EPC]

NDC QR Code

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NDC 0031-8742 QR Code

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.