Home NDC 56062-272 sinus relief
Product NDC 56062-272
11-digit product format 560620272
Labeler code 56062
Product ID 56062-272_bc1f8a1e-1d07-4983-aa27-e259e73e2f32
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen, Phenylephrine HCl
Dosage form TABLET, FILM COATED
Route ORAL
Labeler Publix Super Markets Inc
Application part341
Marketing category OTC MONOGRAPH FINAL
Marketing start 2007-11-26
Marketing end 0000-00-00
Substance ACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE
Active strength 325 mg/1; mg/1
NDC exclude flag No
Listing certified through 2021-12-31
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 · 20 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 56062-272-62 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded product product f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 56062-272-62 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 excluded product product 2ef7874e63bc…57b86245f4fa…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 56062-272-62 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 excluded product product a1b67e2a42f9…c4cf2c586c0d…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 56062-272-62 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 excluded product product cfe11265f3b6…090c488252e2…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 56062-272-62 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 excluded product product cdf11ea48f46…ba0047e9e063…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 56062-272-62 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 excluded product product 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 56062-272-62 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded product product ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 56062-272-62 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 56062-272-62 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 excluded product product ad56d346431e…cc804d4bbf1e…2024-11-09 02:27 UTC · source 2024-11-08 excluded package package 56062-272-62 ad56d346431e…cc804d4bbf1e…
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 RELIEF NON DROWSY (ACETAMINOPHEN, PHENYLEPHRINE HCL) TABLET, FILM COATED [PUBLIX SUPER MARKETS INC] 5 PHENYLEPHRINE HYDROCHLORIDE ACTIVE INGREDIENT 04JA59TNSJ SINUS RELIEF NON DROWSY (ACETAMINOPHEN, PHENYLEPHRINE HCL) TABLET, FILM COATED [PUBLIX SUPER MARKETS INC] 5 ACETAMINOPHEN ACTIVE MOIETY 362O9ITL9D SINUS RELIEF NON DROWSY (ACETAMINOPHEN, PHENYLEPHRINE HCL) TABLET, FILM COATED [PUBLIX SUPER MARKETS INC] 5 PHENYLEPHRINE ACTIVE MOIETY 1WS297W6MV SINUS RELIEF NON DROWSY (ACETAMINOPHEN, PHENYLEPHRINE HCL) TABLET, FILM COATED [PUBLIX SUPER MARKETS INC] 5 ACESULFAME POTASSIUM INACTIVE INGREDIENT 23OV73Q5G9 SINUS RELIEF NON DROWSY (ACETAMINOPHEN, PHENYLEPHRINE HCL) TABLET, FILM COATED [PUBLIX SUPER MARKETS INC] 5 CARNAUBA WAX INACTIVE INGREDIENT R12CBM0EIZ SINUS RELIEF NON DROWSY (ACETAMINOPHEN, PHENYLEPHRINE HCL) TABLET, FILM COATED [PUBLIX SUPER MARKETS INC] 5 CELLULOSE, MICROCRYSTALLINE INACTIVE INGREDIENT OP1R32D61U SINUS RELIEF NON DROWSY (ACETAMINOPHEN, PHENYLEPHRINE HCL) TABLET, FILM COATED [PUBLIX SUPER MARKETS INC] 5 CROSPOVIDONE INACTIVE INGREDIENT 68401960MK SINUS RELIEF NON DROWSY (ACETAMINOPHEN, PHENYLEPHRINE HCL) TABLET, FILM COATED [PUBLIX SUPER MARKETS INC] 5 POLYETHYLENE GLYCOLS INACTIVE INGREDIENT 3WJQ0SDW1A SINUS RELIEF NON DROWSY (ACETAMINOPHEN, PHENYLEPHRINE HCL) TABLET, FILM COATED [PUBLIX SUPER MARKETS INC] 5 POLYVINYL ALCOHOL INACTIVE INGREDIENT 532B59J990 SINUS RELIEF NON DROWSY (ACETAMINOPHEN, PHENYLEPHRINE HCL) TABLET, FILM COATED [PUBLIX SUPER MARKETS INC] 5 POVIDONES INACTIVE INGREDIENT FZ989GH94E SINUS RELIEF NON DROWSY (ACETAMINOPHEN, PHENYLEPHRINE HCL) TABLET, FILM COATED [PUBLIX SUPER MARKETS INC] 5 STEARIC ACID INACTIVE INGREDIENT 4ELV7Z65AP SINUS RELIEF NON DROWSY (ACETAMINOPHEN, PHENYLEPHRINE HCL) TABLET, FILM COATED [PUBLIX SUPER MARKETS INC] 5 TALC INACTIVE INGREDIENT 7SEV7J4R1U SINUS RELIEF NON DROWSY (ACETAMINOPHEN, PHENYLEPHRINE HCL) TABLET, FILM COATED [PUBLIX SUPER MARKETS INC] 5 TITANIUM DIOXIDE INACTIVE INGREDIENT 15FIX9V2JP SINUS RELIEF NON DROWSY (ACETAMINOPHEN, PHENYLEPHRINE HCL) TABLET, FILM COATED [PUBLIX SUPER MARKETS INC] 5
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 56062-272-62 56062027262 12 BLISTER PACK in 1 CARTON (56062-272-62) > 2 TABLET, FILM COATED in 1 BLISTER PACK 12 blister pack 2007-11-26 0000-00-00 No No Current