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 76 of 79 · 1,576 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Acetaminophen Extra Strength ACETAMINOPHEN Aurohealth LLC 03d42892-4465-4089-90a7-cd5f00c35602 2023-11-29 Warnings Exact identifier application number: M013 Acetaminophen Extra Strength ACETAMINOPHEN Aurohealth LLC 57bb1acc-b9a0-48cd-8e5c-33712441ce81 2023-11-29 Warnings Exact identifier application number: M013 Acetaminophen Regular Strength ACETAMINOPHEN Aurohealth LLC cc0ab7a1-e535-4dc8-962f-c58949fc1737 2023-11-29 Warnings Exact identifier application number: M013 Acetaminophen ACETAMINOPHEN Aurohealth LLC a4ff94b9-c248-4cd3-8491-38e9555cc22e 2023-11-29 Warnings Exact identifier application number: M013 Aurophen Extra Strength for Adults ACETAMINOPHEN Aurohealth LLC d59c5f04-4bcc-4a52-a42f-e049506f00de 2023-11-29 Warnings Exact identifier application number: M013 Aurophen Extra Strength for Adults ACETAMINOPHEN Aurohealth LLC a769094b-1e91-4ca7-ba67-21aa7e312910 2023-11-29 Warnings Exact identifier application number: M013 Acetaminophen ACETAMINOPHEN Aurohealth LLC 30756257-f748-4a5d-b031-dd267d0f91ad 2023-11-29 Warnings Exact identifier application number: M013 Aurophen Regular Strength ACETAMINOPHEN Aurohealth LLC 8eda893f-5266-4b7a-95b9-2e194973cf06 2023-11-29 Warnings Exact identifier application number: M013 Childrens Pain Relief ACETAMINOPHEN Aurohealth LLC 00ec6518-b5e3-49d1-a342-139381c3bfd2 2023-11-29 Warnings Exact identifier application number: M013 CHILDRENS PAIN RELIEF ACETAMINOPHEN Better Living Brands, LLC fadb4c09-071f-56c0-e053-6294a90ae6c1 2023-11-28 Warnings Exact identifier application number: M013 Acetaminophen and Diphenhydramine hydrochloride ACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE Better Living Brands, LLC fc07d516-9ffe-9989-e053-6294a90ae1a5 2023-11-28 Warnings Exact identifier application number: M013 NOTTS - Tension Headache ACETAMINOPHEN, CAFFEINE VIVUNT PHARMA LLC 08f2ae03-967b-ad7e-e063-6294a90a8484 2023-11-24 Warnings Exact identifier application number: M013 Sanatos Multi Symptoms Nighttime ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE Pharmadel LLC 0a60326a-a17b-e843-e063-6394a90ac211 2023-11-22 Warnings Exact identifier application number: M013 Sanatos Nighttime Multi Symptoms ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE Pharmadel LLC 0ab188f3-f7f9-d665-e063-6294a90a198a 2023-11-22 Warnings Exact identifier application number: M013 ASPIRIN ASPIRIN TIME CAP LABS INC fe12519c-3e5f-4592-bd34-2d6b81b981f4 2023-11-22 Warnings Exact identifier application number: M013 Rugby Regular Strength Acetaminophen ACETAMINOPHEN A-S Medication Solutions 400d4a29-9e39-4e74-8272-37be5d789924 2023-11-22 Warnings Exact identifier application number: M013 RIGHT REMEDIES Pain Relief Extra Strength Caplet ACETAMINOPHEN Strive Pharmaceuticals Inc. dcce28d9-8528-489e-b995-1d98e9d0e6ad 2023-11-21 Warnings Exact identifier application number: M013 Sanatos Multi Symptom Daytime ACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCI Pharmadel LLC 0ab11691-5b29-55fc-e063-6394a90aa328 2023-11-17 Warnings Exact identifier application number: M013 Acetaminophen ACETAMINOPHEN A-S Medication Solutions 1e223faa-f6d0-4235-bc4c-6cfca84a5b0a 2023-11-17 Warnings Exact identifier application number: M013 SanaTos X ACETAMINOPHEN, DEXTROMETHORPHAN HBR,GUAIFENESIN, PHENYLEPHRINE HCI Pharmadel LLC 85b8ef3d-7318-7f3b-e053-2991aa0a0777 2023-11-14 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