FDA.reportPublic FDA data

Relief-PE

Product NDC
50332-0153
11-digit product format
503320153
Labeler code
50332
Product ID
50332-0153_129bfe8e-117e-4a42-98eb-e25990b3f2a5
Type
HUMAN OTC DRUG
Nonproprietary name
ACETAMINOPHEN, PHENYLEPHRINE, CHLORPHENIRAMINE
Dosage form
TABLET, COATED
Route
ORAL
Labeler
HART Health
Application
M
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2012-04-16
Substance
ACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE; CHLORPHENIRAMINE MALEATE
Active strength
325; 5; 2 mg/1; mg/1; mg/1
Pharmacologic classes
Adrenergic alpha1-Agonists [MoA], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], alpha-1 Adrenergic Agonist [EPC]
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product
Yes
Brand name base
Relief-PE
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ACETAMINOPHEN325 mg/1
PHENYLEPHRINE HYDROCHLORIDE5 mg/1
CHLORPHENIRAMINE MALEATE2 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 3 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
362O9ITL9DInternal UNII lookup
04JA59TNSJInternal UNII lookup
V1Q0O9OJ9ZInternal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
1046781Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
9475fb51-931b-4a89-be6b-62e715d0883eAvailable on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
e4e263da-1c53-440f-bb80-b7a575843b5aProduct name120260313
d2168cac-a261-415a-9c78-3522859fa720Product name320251124
05a8cdd1-eeb8-409e-b938-0778225eca7dProduct name420250221
e5b5c132-b15d-435b-9faa-2f74e5cadcf9Product name820250220
f489e8f3-5c9e-4818-b539-a73587edcfc7Product name220240229
0f7ae452-206d-4fc4-868d-56fc47074084Product name120231011
b5abe2e3-39a1-43eb-9bff-f3c1653fe3dfProduct name220190930
d17a97fa-387f-690e-d2be-0083ab044a03Product name320170725
0fdb98e2-b951-a1ce-5715-2b187ba500efProduct name420170718
e0b6c8be-f2bd-9f86-a9fc-3ed56ffaa814Product name320150910
c6fba691-a132-4ede-95c6-f8c6bd696636Product name120150902
c0200ab5-4954-454e-9676-30b741b245bdProduct name120150730
42f3c020-f1b3-89bc-7bdc-e1f10e680485Product name120140508
e949165d-714d-e548-2b76-0cb5def16f30Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50332-0153-4Relief-PE100 in 1 BOX, UNIT-DOSETABLET, COATED1002
50332-0153-7Relief-PE250 in 1 BOX, UNIT-DOSETABLET, COATED2502

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50332-0153RELIEF-PE (ACETAMINOPHEN, PHENYLEPHRINE, CHLORPHENIRAMINE) TABLET, COATED [HART HEALTH]1Current NDC, 2 package rows20240217_9475fb51-931b-4a89-be6b-62e715d0883e.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 4 of 6 · 111 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
First Street Antibacterial Liquid HandBENZALKONIUM CHLORIDEAmerifoods Trading Companye9d5fefa-970b-42ba-8139-18e5644153442025-11-06WarningsExact identifier
application number: M
CetirzaCETIRIZINE HCLHART Health44b22f6f-5731-4dfe-af33-4e4e54fc3af52025-10-06WarningsExact identifier
application number: M
Dolce and Gabbana Blueberry Nutri Tint SPF 20 6W LightZINC OXIDEDolce & Gabbana Beauty S.R.Ld2930d0e-c622-4843-87f2-fa1a92837ff22025-09-05WarningsExact identifier
application number: M
AlcoholISOPROPYL ALCOHOLNorMed959815e5-a73b-4905-9d7d-904b334983862025-08-15WarningsExact identifier
application number: M
TRIBIOTICBACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATEHART Healthc1903b9f-390a-4756-800c-fd93be4182e32025-08-13Warnings, Adverse reactionsExact identifier
application number: M
THERASTATCHERRY COUGH DROPSHART Health96bae19a-3337-4199-9b8c-cdf9b368178b2025-08-04WarningsExact identifier
application number: M
Docu LiquidDOCUSATE SODIUMATLANTIC BIOLOGICALS CORP.f4ed0721-3be9-4108-a6c9-dbbe115249e92025-07-31WarningsExact identifier
application number: M
MINTOX MAXIMUM STRENGTHALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONEATLANTIC BIOLOGICALS CORP.ac6a47e7-972f-4b82-96da-89926d345e9f2025-07-31WarningsExact identifier
application number: M
SENNASENNAATLANTIC BIOLOGICALS CORP.8b7cc0d5-029b-43f7-a050-8771e7db45512025-07-31WarningsExact identifier
application number: M
Stimulant Laxative Plus Stool SoftenerDOCUSATE SODIUM 50 MG AND SENNOSIDES 8.6 MGATLANTIC BIOLOGICALS CORP.4c02fcec-6bb7-4497-96c5-0d809209dd172025-06-27WarningsExact identifier
application number: M
Orythia Pain Relieving LidocaineLIDOCAINEPlanet (Anhui) Pharmaceutical Co., Ltd.d658d495-dd2c-40b7-9446-6f10040ed55e2025-06-27WarningsExact identifier
application number: M
Bonica EaseX Pain RelievingCAMPHOR (SYNTHETIC), MENTHOL, METHYL SALICYLATEPlanet (Anhui) Pharmaceutical Co., Ltd.34f1196a-fda1-4bef-be71-e5a09ee97bc12025-06-27WarningsExact identifier
application number: M
Regular Strength Enteric coated aspirinASPIRINATLANTIC BIOLOGICALS CORP.e1c8d0ed-da1d-4b1a-9a85-7b8532775f872025-06-24WarningsExact identifier
application number: M
Aspirin Low Dose Chewable OrangeASPIRINATLANTIC BIOLOGICALS CORP.a0d8ee59-1ce0-4ddd-a90c-54adb512540c2025-06-24WarningsExact identifier
application number: M
Hydrogen PeroxideHYDROGEN PEROXIDEHART Healthf50af223-ba83-458a-a557-1ba5dc221a9c2025-06-10WarningsExact identifier
application number: M
Pharbetol Regular strengthACETAMINOPHENATLANTIC BIOLOGICALS CORP.05a91d24-b498-4ba2-a275-68b871cf62d22025-06-05WarningsExact identifier
application number: M
TEENY TUMMY Gas Relief DropsSIMETHICONEATLANTIC BIOLOGICALS CORP376660a2-becb-48cf-a9f5-6a76a8b8ca702025-05-30WarningsExact identifier
application number: M
Mineral OilMINERAL OILATLANTIC BIOLOGICALS CORP.960502ae-2468-406e-8799-cacb01f2727e2025-05-23WarningsExact identifier
application number: M
Stomach Relief Regular StrengthBISMUTH SUBSALICYLATEATLANTIC BIOLOGICALS CORP.5c02d0ba-91e4-4bd2-ac66-6905323653b22025-05-12WarningsExact identifier
application number: M
MAX Tussin Cough and Chest Congestion DM Sugar FreeDEXTROMETHORPHAN HBR, GUAIFENESINATLANTIC BIOLOGICALS CORP.8f496c61-41a6-41ba-80f5-7a5309c4d18b2025-05-12WarningsExact identifier
application number: M

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1046781acetaminophen 325 MG / chlorpheniramine maleate 2 MG / phenylephrine HCl 5 MG Oral TabletPSN9475fb51-931b-4a89-be6b-62e715d0883e2
1046781acetaminophen 325 MG / chlorpheniramine maleate 2 MG / phenylephrine hydrochloride 5 MG Oral TabletSCD9475fb51-931b-4a89-be6b-62e715d0883e2
1046781APAP 325 MG / chlorpheniramine maleate 2 MG / phenylephrine hydrochloride 5 MG Oral TabletSY9475fb51-931b-4a89-be6b-62e715d0883e2

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
50332-0153-450332015304100 TABLET, COATED in 1 BOX, UNIT-DOSE (50332-0153-4) 2012-04-16NoNoCurrent
50332-0153-750332015307250 TABLET, COATED in 1 BOX, UNIT-DOSE (50332-0153-7) 2012-04-16NoNoCurrent