Home NDC 11673-390 Menstrual Relief
Product NDC 11673-390
11-digit product format 116730390
Labeler code 11673
Product ID 11673-390_cdfd3368-2530-43c8-8b63-9051f33bab71
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen, Caffeine and Pyrilamine maleate
Dosage form TABLET, FILM COATED
Route ORAL
Labeler Target Corporation
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-04-01
Marketing end 2028-01-31
Substance ACETAMINOPHEN; CAFFEINE; PYRILAMINE MALEATE
Active strength 500; 60; 15 mg/1; mg/1; mg/1
Pharmacologic classes Central Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE], Methylxanthine [EPC], Xanthines [CS]
NDC exclude flag No
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 Menstrual Relief Active Ingredients# Ingredient, Strength table Ingredient Strength ACETAMINOPHEN 500 mg/1 CAFFEINE 60 mg/1 PYRILAMINE MALEATE 15 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 362O9ITL9D Internal UNII lookup 3G6A5W338E Internal UNII lookup R35D29L3ZA Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1597298 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 11673-390-10 Menstrual Relief 1 in 1 CARTON TABLET, FILM COATED 1 10 11673-390-10 Menstrual Relief 40 in 1 BOTTLE TABLET, FILM COATED 40 10
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded ACETAMINOPHEN ACTIVE INGREDIENT 362O9ITL9D MENSTRUAL RELIEF (ACETAMINOPHEN, CAFFEINE AND PYRILAMINE MALEATE) TABLET [TARGET CORPORATION] 4 CAFFEINE ACTIVE INGREDIENT 3G6A5W338E MENSTRUAL RELIEF (ACETAMINOPHEN, CAFFEINE AND PYRILAMINE MALEATE) TABLET [TARGET CORPORATION] 4 PYRILAMINE MALEATE ACTIVE INGREDIENT R35D29L3ZA MENSTRUAL RELIEF (ACETAMINOPHEN, CAFFEINE AND PYRILAMINE MALEATE) TABLET [TARGET CORPORATION] 4 ACETAMINOPHEN ACTIVE MOIETY 362O9ITL9D MENSTRUAL RELIEF (ACETAMINOPHEN, CAFFEINE AND PYRILAMINE MALEATE) TABLET [TARGET CORPORATION] 4 CAFFEINE ACTIVE MOIETY 3G6A5W338E MENSTRUAL RELIEF (ACETAMINOPHEN, CAFFEINE AND PYRILAMINE MALEATE) TABLET [TARGET CORPORATION] 4 PYRILAMINE ACTIVE MOIETY HPE317O9TL MENSTRUAL RELIEF (ACETAMINOPHEN, CAFFEINE AND PYRILAMINE MALEATE) TABLET [TARGET CORPORATION] 4 CROSCARMELLOSE SODIUM INACTIVE INGREDIENT M28OL1HH48 MENSTRUAL RELIEF (ACETAMINOPHEN, CAFFEINE AND PYRILAMINE MALEATE) TABLET [TARGET CORPORATION] 4 HYPROMELLOSES INACTIVE INGREDIENT 3NXW29V3WO MENSTRUAL RELIEF (ACETAMINOPHEN, CAFFEINE AND PYRILAMINE MALEATE) TABLET [TARGET CORPORATION] 4 MAGNESIUM STEARATE INACTIVE INGREDIENT 70097M6I30 MENSTRUAL RELIEF (ACETAMINOPHEN, CAFFEINE AND PYRILAMINE MALEATE) TABLET [TARGET CORPORATION] 4 POLYDEXTROSE INACTIVE INGREDIENT VH2XOU12IE MENSTRUAL RELIEF (ACETAMINOPHEN, CAFFEINE AND PYRILAMINE MALEATE) TABLET [TARGET CORPORATION] 4 POLYETHYLENE GLYCOLS INACTIVE INGREDIENT 3WJQ0SDW1A MENSTRUAL RELIEF (ACETAMINOPHEN, CAFFEINE AND PYRILAMINE MALEATE) TABLET [TARGET CORPORATION] 4 STEARIC ACID INACTIVE INGREDIENT 4ELV7Z65AP MENSTRUAL RELIEF (ACETAMINOPHEN, CAFFEINE AND PYRILAMINE MALEATE) TABLET [TARGET CORPORATION] 4 TITANIUM DIOXIDE INACTIVE INGREDIENT 15FIX9V2JP MENSTRUAL RELIEF (ACETAMINOPHEN, CAFFEINE AND PYRILAMINE MALEATE) TABLET [TARGET CORPORATION] 4 TRIACETIN INACTIVE INGREDIENT XHX3C3X673 MENSTRUAL RELIEF (ACETAMINOPHEN, CAFFEINE AND PYRILAMINE MALEATE) TABLET [TARGET CORPORATION] 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 11673-390 MENSTRUAL RELIEF (ACETAMINOPHEN, CAFFEINE AND PYRILAMINE MALEATE) TABLET, FILM COATED [TARGET CORPORATION] 8 Current NDC, 2 package rows 20250110_bc65e205-64fd-4764-8c5e-2793af4e9adf.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 47 of 79 · 1,579 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join GOOD REMEDIES Extra Strength Pain Relief PM Caplet ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE Strive Pharmaceuticals Inc. 2d642d8e-c154-a970-e063-6294a90a03bf 2025-03-14 Warnings Exact identifier application number: M013 Pain Relief ACETAMINOPHEN DISCOUNT DRUG MART 97f78c4a-9d0d-4fe1-8b2b-d5f8ab939ac4 2025-03-07 Warnings Exact identifier application number: M013 Redicare Non-Aspirin 500mg REDICARE NON-ASPIRIN, ACETAMINOPHEN 500MG Redicare LLC 2f229898-1777-732c-e063-6394a90a76bc 2025-03-04 Warnings, Adverse reactions Exact identifier application number: M013 Major Extra Strength Acetaminophen Liquid ACETAMINOPHEN Major Pharmaceuticals 2f3af4dd-45d5-87b4-e063-6294a90ab3cc 2025-02-28 Warnings Exact identifier application number: M013 LOW DOSE ASPIRIN ASPIRIN NCS HealthCare of KY, LLC dba Vangard Labs ed9a71d6-a56e-416a-bb89-6d41307efc5a 2025-02-27 Warnings Exact identifier application number: M013 Aspirin ASPIRIN PD-Rx Pharmaceuticals, Inc. 77429b7f-78e4-42c0-8679-ae8da1748848 2025-02-26 Warnings Exact identifier application number: M013 AeroTab Non-Aspirin ACETAMINOPHEN 500MG ES Aero Healthcare faa3a4ef-3c70-06ca-e053-6394a90a512d 2025-02-26 Warnings Exact identifier application number: M013 Bufferin Regular Strength Pain Relief ASPIRIN Genomma Lab USA 3543b2bf-1062-468a-a5dc-eabb2408af8c 2025-02-25 Warnings Exact identifier application number: M013 Calmour Childrens Acetaminophen Strips Chewable ACETAMINOPHEN ORAL CHEWABLE 80 MG Calmour ae47b027-4f29-45bb-a8bd-812978932835 2025-02-22 Warnings Exact identifier application number: M013 Infants TYLENOL ACETAMINOPHEN Kenvue Brands LLC f9de7c2f-016b-4f40-8b5e-141ad194be97 2025-02-20 Warnings Exact identifier application number: M013 Genexa Acetaminophen PM Extra Strength ACETAMINOPHEN Genexa Inc. d82cf6f3-a291-ca2b-e053-2a95a90a6de1 2025-02-20 Warnings Exact identifier application number: M013 Childrens Acetaminophen ACETAMINOPHEN Advagen Pharma Limited 8b9456c9-a56b-4748-adb8-c66d6bf072e8 2025-02-19 Warnings Exact identifier application number: M013 Genexa Childrens Acetaminophen ACETAMINOPHEN Genexa Inc. d89fd9d8-d88e-3968-e053-2a95a90afc5f 2025-02-19 Warnings Exact identifier application number: M013 Acetaminophen ACETAMINOPHEN Precision Dose, Inc. debfa787-7a48-48b5-94b0-612820524032 2025-02-19 Warnings Exact identifier application number: M013 Acetaminophen ACETAMINOPHEN Precision Dose, Inc. b16e5dcf-b290-4ff2-a150-4b875647ec9a 2025-02-19 Warnings Exact identifier application number: M013 TYLENOL Extra Strength ACETAMINOPHEN Kenvue Brands LLC bb6533e5-e6a9-488c-b8ab-a6a06e87ede9 2025-02-18 Warnings Exact identifier application number: M013 TYLENOL Extra Strength ACETAMINOPHEN Kenvue Brands LLC c830320e-72ba-48ff-a4cd-250ac5650bf0 2025-02-18 Warnings Exact identifier application number: M013 Aspirina Caplets ASPIRIN Bayer HealthCare LLC. 2e6f5ba8-8e8b-6059-e063-6394a90adcd5 2025-02-18 Warnings Exact identifier application number: M013 Acetaminophen ACETAMINOPHEN PD-Rx Pharmaceuticals, Inc. da7d95af-6583-429d-8d04-e0424f32e9ad 2025-02-17 Warnings Exact identifier application number: M013 GOODYS Mental Alert ASPIRIN AND CAFFEINE Medtech Products Inc. 31ef6d07-d314-4d09-abcd-389ba66cbcc5 2025-02-17 Warnings Exact identifier application number: M013
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 11673-390-10 11673039010 1 BOTTLE in 1 CARTON (11673-390-10) / 40 TABLET, FILM COATED in 1 BOTTLE 1 bottle 2019-04-01 2028-01-31 No No Historical