Home NDC 55910-033-09 Mucus Relief Cold and Sinus
Product NDC 55910-033
Requested package NDC 55910-033-09
11-digit product format 559100033
Labeler code 55910
Product ID 55910-033_66e4807c-3e92-44d7-b586-d31b41b3d2a9
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen, Guaifenesin, Phenylephrine HCl
Dosage form LIQUID
Route ORAL
Labeler Dolgencorp, Inc. (DOLLAR GENERAL & REXALL)
Application part341
Marketing category OTC MONOGRAPH FINAL
Marketing start 2014-06-30
Marketing end 2025-01-31
Substance ACETAMINOPHEN; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
Active strength 650 mg/20mL; mg/20mL; mg/20mL
Pharmacologic classes Adrenergic alpha1-Agonists [MoA], Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE], alpha-1 Adrenergic Agonist [EPC]
NDC exclude flag No
Listing certified through 0000-00-00
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 · 6 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…
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 ACETAMINOPHEN ACTIVE INGREDIENT 362O9ITL9D MUCUS RELIEF COLD AND SINUS MAXIMUM STRENGTH (ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL) LIQUID [DOLGENCORP, INC. (DOLLAR GENERAL & REXALL)] 3 GUAIFENESIN ACTIVE INGREDIENT 495W7451VQ MUCUS RELIEF COLD AND SINUS MAXIMUM STRENGTH (ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL) LIQUID [DOLGENCORP, INC. (DOLLAR GENERAL & REXALL)] 3 PHENYLEPHRINE HYDROCHLORIDE ACTIVE INGREDIENT 04JA59TNSJ MUCUS RELIEF COLD AND SINUS MAXIMUM STRENGTH (ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL) LIQUID [DOLGENCORP, INC. (DOLLAR GENERAL & REXALL)] 3 ACETAMINOPHEN ACTIVE MOIETY 362O9ITL9D MUCUS RELIEF COLD AND SINUS MAXIMUM STRENGTH (ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL) LIQUID [DOLGENCORP, INC. (DOLLAR GENERAL & REXALL)] 3 GUAIFENESIN ACTIVE MOIETY 495W7451VQ MUCUS RELIEF COLD AND SINUS MAXIMUM STRENGTH (ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL) LIQUID [DOLGENCORP, INC. (DOLLAR GENERAL & REXALL)] 3 PHENYLEPHRINE ACTIVE MOIETY 1WS297W6MV MUCUS RELIEF COLD AND SINUS MAXIMUM STRENGTH (ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL) LIQUID [DOLGENCORP, INC. (DOLLAR GENERAL & REXALL)] 3 ANHYDROUS CITRIC ACID INACTIVE INGREDIENT XF417D3PSL MUCUS RELIEF COLD AND SINUS MAXIMUM STRENGTH (ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL) LIQUID [DOLGENCORP, INC. (DOLLAR GENERAL & REXALL)] 3 EDETATE DISODIUM INACTIVE INGREDIENT 7FLD91C86K MUCUS RELIEF COLD AND SINUS MAXIMUM STRENGTH (ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL) LIQUID [DOLGENCORP, INC. (DOLLAR GENERAL & REXALL)] 3 FD&C BLUE NO. 1 INACTIVE INGREDIENT H3R47K3TBD MUCUS RELIEF COLD AND SINUS MAXIMUM STRENGTH (ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL) LIQUID [DOLGENCORP, INC. (DOLLAR GENERAL & REXALL)] 3 FD&C RED NO. 40 INACTIVE INGREDIENT WZB9127XOA MUCUS RELIEF COLD AND SINUS MAXIMUM STRENGTH (ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL) LIQUID [DOLGENCORP, INC. (DOLLAR GENERAL & REXALL)] 3 GLYCERIN INACTIVE INGREDIENT PDC6A3C0OX MUCUS RELIEF COLD AND SINUS MAXIMUM STRENGTH (ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL) LIQUID [DOLGENCORP, INC. (DOLLAR GENERAL & REXALL)] 3 PROPYL GALLATE INACTIVE INGREDIENT 8D4SNN7V92 MUCUS RELIEF COLD AND SINUS MAXIMUM STRENGTH (ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL) LIQUID [DOLGENCORP, INC. (DOLLAR GENERAL & REXALL)] 3 PROPYLENE GLYCOL INACTIVE INGREDIENT 6DC9Q167V3 MUCUS RELIEF COLD AND SINUS MAXIMUM STRENGTH (ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL) LIQUID [DOLGENCORP, INC. (DOLLAR GENERAL & REXALL)] 3 SODIUM BENZOATE INACTIVE INGREDIENT OJ245FE5EU MUCUS RELIEF COLD AND SINUS MAXIMUM STRENGTH (ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL) LIQUID [DOLGENCORP, INC. (DOLLAR GENERAL & REXALL)] 3 SORBITOL INACTIVE INGREDIENT 506T60A25R MUCUS RELIEF COLD AND SINUS MAXIMUM STRENGTH (ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL) LIQUID [DOLGENCORP, INC. (DOLLAR GENERAL & REXALL)] 3 SUCRALOSE INACTIVE INGREDIENT 96K6UQ3ZD4 MUCUS RELIEF COLD AND SINUS MAXIMUM STRENGTH (ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL) LIQUID [DOLGENCORP, INC. (DOLLAR GENERAL & REXALL)] 3 TRISODIUM CITRATE DIHYDRATE INACTIVE INGREDIENT B22547B95K MUCUS RELIEF COLD AND SINUS MAXIMUM STRENGTH (ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL) LIQUID [DOLGENCORP, INC. (DOLLAR GENERAL & REXALL)] 3 WATER INACTIVE INGREDIENT 059QF0KO0R MUCUS RELIEF COLD AND SINUS MAXIMUM STRENGTH (ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL) LIQUID [DOLGENCORP, INC. (DOLLAR GENERAL & REXALL)] 3 XANTHAN GUM INACTIVE INGREDIENT TTV12P4NEE MUCUS RELIEF COLD AND SINUS MAXIMUM STRENGTH (ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL) LIQUID [DOLGENCORP, INC. (DOLLAR GENERAL & REXALL)] 3
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 55910-033-09 55910003309 266 mL in 1 BOTTLE, PLASTIC (55910-033-09) 266 ml 2014-06-30 2025-01-31 No No Current