Home NDC 11673-628-09 Sinus Pressure and Pain Relief
Product NDC 11673-628
Requested package NDC 11673-628-09
11-digit product format 116730628
Labeler code 11673
Product ID 11673-628_44655f9b-9f49-4372-b4ec-f6c8ada5f16c
Type HUMAN OTC DRUG
Nonproprietary name acetaminophen, guaifenesin, phenylephrine HCl
Dosage form TABLET
Route ORAL
Labeler Target Corporation
Application part341
Marketing category OTC MONOGRAPH FINAL
Marketing start 2013-05-03
Marketing end 2021-06-26
Substance ACETAMINOPHEN; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
Active strength 325 mg/1; mg/1; mg/1
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 · 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 ACETAMINOPHEN ACTIVE INGREDIENT 362O9ITL9D SINUS PRESSURE AND PAIN RELIEF EXTRA STRENGTH (ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL) TABLET [TARGET CORPORATION] 1 GUAIFENESIN ACTIVE INGREDIENT 495W7451VQ SINUS PRESSURE AND PAIN RELIEF EXTRA STRENGTH (ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL) TABLET [TARGET CORPORATION] 1 PHENYLEPHRINE HYDROCHLORIDE ACTIVE INGREDIENT 04JA59TNSJ SINUS PRESSURE AND PAIN RELIEF EXTRA STRENGTH (ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL) TABLET [TARGET CORPORATION] 1 ACETAMINOPHEN ACTIVE MOIETY 362O9ITL9D SINUS PRESSURE AND PAIN RELIEF EXTRA STRENGTH (ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL) TABLET [TARGET CORPORATION] 1 GUAIFENESIN ACTIVE MOIETY 495W7451VQ SINUS PRESSURE AND PAIN RELIEF EXTRA STRENGTH (ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL) TABLET [TARGET CORPORATION] 1 PHENYLEPHRINE ACTIVE MOIETY 1WS297W6MV SINUS PRESSURE AND PAIN RELIEF EXTRA STRENGTH (ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL) TABLET [TARGET CORPORATION] 1 CROSPOVIDONE INACTIVE INGREDIENT 68401960MK SINUS PRESSURE AND PAIN RELIEF EXTRA STRENGTH (ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL) TABLET [TARGET CORPORATION] 1 D&C YELLOW NO. 10 INACTIVE INGREDIENT 35SW5USQ3G SINUS PRESSURE AND PAIN RELIEF EXTRA STRENGTH (ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL) TABLET [TARGET CORPORATION] 1 FD&C YELLOW NO. 6 INACTIVE INGREDIENT H77VEI93A8 SINUS PRESSURE AND PAIN RELIEF EXTRA STRENGTH (ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL) TABLET [TARGET CORPORATION] 1 MAGNESIUM STEARATE INACTIVE INGREDIENT 70097M6I30 SINUS PRESSURE AND PAIN RELIEF EXTRA STRENGTH (ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL) TABLET [TARGET CORPORATION] 1 MALTODEXTRIN INACTIVE INGREDIENT 7CVR7L4A2D SINUS PRESSURE AND PAIN RELIEF EXTRA STRENGTH (ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL) TABLET [TARGET CORPORATION] 1 POLYETHYLENE GLYCOLS INACTIVE INGREDIENT 3WJQ0SDW1A SINUS PRESSURE AND PAIN RELIEF EXTRA STRENGTH (ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL) TABLET [TARGET CORPORATION] 1 POLYVINYL ALCOHOL INACTIVE INGREDIENT 532B59J990 SINUS PRESSURE AND PAIN RELIEF EXTRA STRENGTH (ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL) TABLET [TARGET CORPORATION] 1 POVIDONES INACTIVE INGREDIENT FZ989GH94E SINUS PRESSURE AND PAIN RELIEF EXTRA STRENGTH (ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL) TABLET [TARGET CORPORATION] 1 SODIUM STARCH GLYCOLATE TYPE B POTATO INACTIVE INGREDIENT 27NA468985 SINUS PRESSURE AND PAIN RELIEF EXTRA STRENGTH (ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL) TABLET [TARGET CORPORATION] 1 STARCH, CORN INACTIVE INGREDIENT O8232NY3SJ SINUS PRESSURE AND PAIN RELIEF EXTRA STRENGTH (ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL) TABLET [TARGET CORPORATION] 1 STEARIC ACID INACTIVE INGREDIENT 4ELV7Z65AP SINUS PRESSURE AND PAIN RELIEF EXTRA STRENGTH (ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL) TABLET [TARGET CORPORATION] 1 TALC INACTIVE INGREDIENT 7SEV7J4R1U SINUS PRESSURE AND PAIN RELIEF EXTRA STRENGTH (ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL) TABLET [TARGET CORPORATION] 1 TITANIUM DIOXIDE INACTIVE INGREDIENT 15FIX9V2JP SINUS PRESSURE AND PAIN RELIEF EXTRA STRENGTH (ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL) TABLET [TARGET CORPORATION] 1
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 11673-628-09 11673062809 2 BLISTER PACK in 1 CARTON (11673-628-09) > 10 TABLET in 1 BLISTER PACK 2 blister pack 2013-05-03 2021-06-26 No No Current