Home NDC 51316-390 MENSTRUAL RELIEF
Product NDC 51316-390
11-digit product format 513160390
Labeler code 51316
Product ID 51316-390_8ac4bd2d-c57b-4f42-92f3-4d662718ef11
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen, Caffeine, Pyrilamine maleate
Dosage form TABLET, FILM COATED
Route ORAL
Labeler CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED
Application M027
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-05-11
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
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 MENSTRUAL RELIEF
Listing expiration 2027-12-31 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 51316-390-10 MENSTRUAL RELIEF 1 in 1 CARTON TABLET, FILM COATED 1 2 51316-390-10 MENSTRUAL RELIEF 40 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 40 2 51316-390-21 MENSTRUAL RELIEF 8 in 1 BLISTER PACK TABLET, FILM COATED 8 2 51316-390-21 MENSTRUAL RELIEF 2 in 1 CARTON TABLET, FILM COATED 2 2
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 3 of 3 · 43 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 51316-390-10 51316039010 1 BOTTLE, PLASTIC in 1 CARTON (51316-390-10) / 40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC 2026-05-11 No No Current 51316-390-21 51316039021 2 BLISTER PACK in 1 CARTON (51316-390-21) / 8 TABLET, FILM COATED in 1 BLISTER PACK 2 blister pack 2026-05-11 No No Current