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 23 of 79 · 1,579 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Aspirin 81 mg ASPIRIN HYVEE INC 3e602287-565e-a5b9-e063-6294a90abc17 2026-01-13 Warnings Exact identifier application number: M013 ASPIRIN DELAYED RELEASE 81MG ASPIRIN DELAYED RELEASE 81MG Farmacias De Similares TX LLC 3a8a3efc-f0b3-411c-e063-6394a90a84b7 2026-01-13 Warnings Exact identifier application number: M013 Chewable Aspirin 81 mg ASPIRIN HYVEE INC 459f749f-9d23-8752-e063-6394a90a8c81 2026-01-13 Warnings Exact identifier application number: M013 ASPIRIN 325 mg ASPIRIN HYVEE INC 459d01df-6ff6-cff6-e063-6394a90ab35c 2026-01-13 Warnings Exact identifier application number: M013 Pain Terminator Extra Strength Pain Relief CAFFEINE, ACETAMINOPHEN, ASPIRIN Wildman Business Group 8ffb02d9-92df-4d2f-a367-1c71490807fb 2026-01-12 Warnings Exact identifier application number: M013 Aspirin Packs ASPIRIN Sina Health Inc 2865a2c3-53fc-ab9a-e063-6394a90a1418 2026-01-12 Warnings Exact identifier application number: M013 Acetaminophen ACETAMINOPHEN PD-Rx Pharmaceuticals, Inc. 64696f65-415e-4ce1-a5b3-70662fbcb002 2026-01-12 Warnings Exact identifier application number: M013 Aspirin enteric coated low dose ASPIRIN Walgreen Company 186a6270-e3de-4499-88a4-5f723fee3e34 2026-01-12 Warnings Exact identifier application number: M013 Tension Headache ACETAMINOPHEN, CAFFEINE Cardinal Health 110, LLC. DBA Leader 96684e3f-a13e-49c3-b437-d2627e528a2d 2026-01-12 Warnings Exact identifier application number: M013 Low Dose Aspirin ASPIRIN Family Dollar Services Inc d35d798e-76f1-454d-86f6-ad11c3bf17d8 2026-01-12 Warnings Exact identifier application number: M013 Xpect Acetaminophen ACETAMINOPHEN Cintas Corporation f4aed854-730e-493d-b523-122156e08dde 2026-01-09 Warnings Exact identifier application number: M013 Aspirin ASPIRIN INVAHEALTH INC e5e8a8d5-9174-7975-e053-2a95a90a9aa6 2026-01-08 Warnings Exact identifier application number: M013 Xpect Cold Relief ACETAMINOPHEN GUAIFENESEIN PHENYLEPHRINE HCL Cintas Corporation 02391d55-32b2-4083-9315-98e9b3650c55 2026-01-08 Warnings Exact identifier application number: M013 pain relief back and body EXTRA STRENGTH ASPIRIN, CAFFEINE Rite Aid Corporation a71392c8-3f5b-4d00-baba-a4055ed68bc1 2026-01-07 Warnings Exact identifier application number: M013 Pain Reliever Extra Strength ACETAMINOPHEN L.N.K. International, Inc. 8fed703a-9de2-4c76-a783-fcf004f9b890 2026-01-07 Warnings Exact identifier application number: M013 Aspirin ASPIRIN Amerisource Bergen c3099892-a8cd-4574-a6f9-041e59e2feae 2026-01-07 Warnings Exact identifier application number: M013 Bactimicina Childrens Pain and Fever ACETAMINOPHEN DLC Laboratories, Inc. bdade270-d813-4178-b594-4951632b6839 2026-01-07 Warnings Exact identifier application number: M013 Goodmeds Extra Strength Pain Relief PM ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE Cabinet Health P.B.C. 02c60967-46d7-49b7-82be-bc3c5fd36484 2026-01-06 Warnings Exact identifier application number: M013 Childrens Acetaminophen ACETAMINOPHEN ARMY AND AIR FORCE EXCHANGE SERVICE a73f8217-9eae-4e2a-b29c-7de3861d0e37 2026-01-06 Warnings Exact identifier application number: M013 Pain Relief Acetaminophen PM ACETAMINOPHEN AND DIPHENHYDRAMINE HCL Rite Aid Corporation f77f0120-4042-4b11-ba9c-cd35e1cd0bee 2026-01-05 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