sinus relief

Product NDC
56062-272
Requested package NDC
56062-272-62
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

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage56062-27256062-272-62DDiscontinued by firm2026-10-05

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 · 10 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Snapshot, Source SHA-256 table
Captured / source dateSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26f5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-312ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-28a1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-21cfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-10cdf11ea48f46…ba0047e9e063…
2025-02-02 03:52 UTC · source 2025-01-31302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-20ed331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-100efc9e666f02…f202fb6c5f17…
2024-11-09 02:27 UTC · source 2024-11-08ad56d346431e…cc804d4bbf1e…

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
56062-272-62EA - Each56062-272edfc5ccd-e769-406f-ae39-b9da3d79210812012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ACETAMINOPHENACTIVE INGREDIENT362O9ITL9DSINUS RELIEF NON DROWSY (ACETAMINOPHEN, PHENYLEPHRINE HCL) TABLET, FILM COATED [PUBLIX SUPER MARKETS INC]5
PHENYLEPHRINE HYDROCHLORIDEACTIVE INGREDIENT04JA59TNSJSINUS RELIEF NON DROWSY (ACETAMINOPHEN, PHENYLEPHRINE HCL) TABLET, FILM COATED [PUBLIX SUPER MARKETS INC]5
ACETAMINOPHENACTIVE MOIETY362O9ITL9DSINUS RELIEF NON DROWSY (ACETAMINOPHEN, PHENYLEPHRINE HCL) TABLET, FILM COATED [PUBLIX SUPER MARKETS INC]5
PHENYLEPHRINEACTIVE MOIETY1WS297W6MVSINUS RELIEF NON DROWSY (ACETAMINOPHEN, PHENYLEPHRINE HCL) TABLET, FILM COATED [PUBLIX SUPER MARKETS INC]5
ACESULFAME POTASSIUMINACTIVE INGREDIENT23OV73Q5G9SINUS RELIEF NON DROWSY (ACETAMINOPHEN, PHENYLEPHRINE HCL) TABLET, FILM COATED [PUBLIX SUPER MARKETS INC]5
CARNAUBA WAXINACTIVE INGREDIENTR12CBM0EIZSINUS RELIEF NON DROWSY (ACETAMINOPHEN, PHENYLEPHRINE HCL) TABLET, FILM COATED [PUBLIX SUPER MARKETS INC]5
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61USINUS RELIEF NON DROWSY (ACETAMINOPHEN, PHENYLEPHRINE HCL) TABLET, FILM COATED [PUBLIX SUPER MARKETS INC]5
CROSPOVIDONEINACTIVE INGREDIENT68401960MKSINUS RELIEF NON DROWSY (ACETAMINOPHEN, PHENYLEPHRINE HCL) TABLET, FILM COATED [PUBLIX SUPER MARKETS INC]5
POLYETHYLENE GLYCOLSINACTIVE INGREDIENT3WJQ0SDW1ASINUS RELIEF NON DROWSY (ACETAMINOPHEN, PHENYLEPHRINE HCL) TABLET, FILM COATED [PUBLIX SUPER MARKETS INC]5
POLYVINYL ALCOHOLINACTIVE INGREDIENT532B59J990SINUS RELIEF NON DROWSY (ACETAMINOPHEN, PHENYLEPHRINE HCL) TABLET, FILM COATED [PUBLIX SUPER MARKETS INC]5
POVIDONESINACTIVE INGREDIENTFZ989GH94ESINUS RELIEF NON DROWSY (ACETAMINOPHEN, PHENYLEPHRINE HCL) TABLET, FILM COATED [PUBLIX SUPER MARKETS INC]5
STEARIC ACIDINACTIVE INGREDIENT4ELV7Z65APSINUS RELIEF NON DROWSY (ACETAMINOPHEN, PHENYLEPHRINE HCL) TABLET, FILM COATED [PUBLIX SUPER MARKETS INC]5
TALCINACTIVE INGREDIENT7SEV7J4R1USINUS RELIEF NON DROWSY (ACETAMINOPHEN, PHENYLEPHRINE HCL) TABLET, FILM COATED [PUBLIX SUPER MARKETS INC]5
TITANIUM DIOXIDEINACTIVE INGREDIENT15FIX9V2JPSINUS RELIEF NON DROWSY (ACETAMINOPHEN, PHENYLEPHRINE HCL) TABLET, FILM COATED [PUBLIX SUPER MARKETS INC]5

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
56062-272-625606202726212 BLISTER PACK in 1 CARTON (56062-272-62) > 2 TABLET, FILM COATED in 1 BLISTER PACK12 blister pack2007-11-260000-00-00NoNoCurrent