60258-530 : Dex-tuss Oral Liquid


NDC: 60258-530
Labeler: Cypress Pharmaceutical, Inc.
Product Type: Human OTC Drug
Drug Name: Dex-tuss
Dosage Form: Oral Liquid
Application #: part341
Rev. Date: 
CSA Schedule: CV (US) [1]


[1] Schedule V Controlled Substance: Low potential for abuse relative to substances listed in Schedule IV and consist primarily of preparations containing limited quantities of certain narcotics. (i.e. Cough preparations containing not more than 200 milligrams of Codeine per 100 milliliters or per 100 grams [such as Robitussin AC, Phenergan with Codeine], and Ezogabine). More Details: US Dept of Justice Controlled Substance Schedules.

NDC Package Codes:

  • 60258-530-16: 473 ML IN 1 BOTTLE (60258‑530‑16)

Active Ingredients:

  • Codeine Phosphate
  • Guaifenesin

Dosage Strength:

  • 10 mg/5mL
  • 300 mg/5mL

NDC QR Code

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NDC 60258-530 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.