Home NDC 59779-919-26 tussin dm
Product NDC 59779-919
Requested package NDC 59779-919-26
11-digit product format 597790919
Labeler code 59779
Product ID 59779-919_ba7142af-ffcd-47ad-864f-9dd9abc6b730
Type HUMAN OTC DRUG
Nonproprietary name Dextromethorphan HBr, Guaifenesin
Dosage form SOLUTION
Route ORAL
Labeler CVS Pharmacy
Application part341
Marketing category OTC MONOGRAPH FINAL
Marketing start 1994-12-07
Marketing end 0000-00-00
Substance DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
Active strength 20 mg/10mL; mg/10mL
Pharmacologic classes 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]
NDC exclude flag No
Listing certified through 2023-12-31
Current FDA listing Historical FDA.report record Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 12 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded DEXTROMETHORPHAN HYDROBROMIDE ACTIVE INGREDIENT 9D2RTI9KYH TUSSIN DM (DEXTROMETHORPHAN HBR, GUAIFENESIN) SOLUTION [CVS PHARMACY] 4 GUAIFENESIN ACTIVE INGREDIENT 495W7451VQ TUSSIN DM (DEXTROMETHORPHAN HBR, GUAIFENESIN) SOLUTION [CVS PHARMACY] 4 DEXTROMETHORPHAN ACTIVE MOIETY 7355X3ROTS TUSSIN DM (DEXTROMETHORPHAN HBR, GUAIFENESIN) SOLUTION [CVS PHARMACY] 4 GUAIFENESIN ACTIVE MOIETY 495W7451VQ TUSSIN DM (DEXTROMETHORPHAN HBR, GUAIFENESIN) SOLUTION [CVS PHARMACY] 4 ASPARTAME INACTIVE INGREDIENT Z0H242BBR1 TUSSIN DM (DEXTROMETHORPHAN HBR, GUAIFENESIN) SOLUTION [CVS PHARMACY] 4 BENZOIC ACID INACTIVE INGREDIENT 8SKN0B0MIM TUSSIN DM (DEXTROMETHORPHAN HBR, GUAIFENESIN) SOLUTION [CVS PHARMACY] 4 GLYCERIN INACTIVE INGREDIENT PDC6A3C0OX TUSSIN DM (DEXTROMETHORPHAN HBR, GUAIFENESIN) SOLUTION [CVS PHARMACY] 4 MENTHOL INACTIVE INGREDIENT L7T10EIP3A TUSSIN DM (DEXTROMETHORPHAN HBR, GUAIFENESIN) SOLUTION [CVS PHARMACY] 4 POLYETHYLENE GLYCOLS INACTIVE INGREDIENT 3WJQ0SDW1A TUSSIN DM (DEXTROMETHORPHAN HBR, GUAIFENESIN) SOLUTION [CVS PHARMACY] 4 WATER INACTIVE INGREDIENT 059QF0KO0R TUSSIN DM (DEXTROMETHORPHAN HBR, GUAIFENESIN) SOLUTION [CVS PHARMACY] 4
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 59779-919-26 59779091926 1 BOTTLE in 1 CARTON (59779-919-26) > 118 mL in 1 BOTTLE 1 bottle 1994-12-07 0000-00-00 No No Current