Menstrual Complete

Product NDC: 11822-0390
11-digit product format: 118220390
Labeler code: 11822
Product ID: 11822-0390_2897863b-f6ec-4b54-add1-2ae7d960e7b9
Type: HUMAN OTC DRUG
Nonproprietary name: Acetaminophen, Caffeine and Pyrilamine maleate
Dosage form: TABLET, FILM COATED
Route: ORAL
Labeler: Rite Aid Corporation
Application: M013
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2002-04-29
Marketing end: 2027-05-30
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

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	11822-0390	11822-0390-8	D	Discontinued by firm		2026-10-23

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 12 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Snapshot, Source SHA-256 table
Captured / source date	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	`557ba5c1ecfa…`	`9c80585c8c6e…`

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 Complete
Brand name suffix: Maximum Strength

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.

Identifier, FDA.report destination table
Identifier	FDA.report destination
69bda7d7-8660-4e8d-b8ac-892a3b1f2124	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
7dea7767-9f52-b60a-5435-33cb9cc28bae	Product name	4	20250124
6338270f-96cb-0ecb-6fbb-0a9bc78001f4	Product name	7	20250116
0ca83774-3f79-b837-5d6f-c210102f3bc8	Product name	6	20250114
41b814f3-0166-1c53-c9ef-a0794c7daf9d	Product name	3	20221110
a590be26-846c-8659-a5a1-fb25907965dc	Product name	2	20221110
2dc76302-91c0-4c35-ad78-99adfb049c4b	Product name	1	20200603
e6065d4b-5ae1-476f-a40e-f2851cbb5d2b	Product name	2	20180221
f212291f-05fe-9603-fc7e-bd73e38ce1e6	Product name	2	20161129
182f9ab4-4ab5-c449-200f-87ce2ce8e550	Product name	2	20151105
332e86c3-7875-ca6e-f934-2206d2b31996	Product name	1	20140508
56625fcc-aa34-9d30-d0e9-1c1beb37ea21	Product name	1	20140508
7dfac40f-a405-cd2e-7c06-3059ec0e1092	Product name	1	20140508
96c2be53-8e44-452d-56a2-d255b2f1af2d	Product name	1	20140508
bf8bd5f7-495f-4022-2780-7ded7ea7ea44	Product name	1	20140508
d223c173-c39b-d764-47d4-d671d3088815	Product name	1	20140508
e01133ad-4dcd-c7f3-454b-2ff569ee160a	Product name	1	20140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
11822-0390-1	Menstrual CompleteMaximum Strength	1 in 1 CARTON	TABLET, FILM COATED	1	32
11822-0390-1	Menstrual CompleteMaximum Strength	40 in 1 BOTTLE, PLASTIC	TABLET, FILM COATED	40	32
11822-0390-8	Menstrual CompleteMaximum Strength	3 in 1 CARTON	TABLET, FILM COATED	3	32
11822-0390-8	Menstrual CompleteMaximum Strength	24 in 1 BLISTER PACK	TABLET, FILM COATED	24	32
11822-0390-9	Menstrual CompleteMaximum Strength	1 in 1 CARTON	TABLET, FILM COATED	1	32
11822-0390-9	Menstrual CompleteMaximum Strength	24 in 1 BOTTLE, PLASTIC	TABLET, FILM COATED	24	32

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
ACETAMINOPHEN	ACTIVE INGREDIENT	362O9ITL9D	MENSTRUAL COMPLETE MAXIMUM STRENGTH (ACETAMINOPHEN, CAFFEINE AND PYRILAMINE MALEATE) TABLET [RITE AID]	14
CAFFEINE	ACTIVE INGREDIENT	3G6A5W338E	MENSTRUAL COMPLETE MAXIMUM STRENGTH (ACETAMINOPHEN, CAFFEINE AND PYRILAMINE MALEATE) TABLET [RITE AID]	14
PYRILAMINE MALEATE	ACTIVE INGREDIENT	R35D29L3ZA	MENSTRUAL COMPLETE MAXIMUM STRENGTH (ACETAMINOPHEN, CAFFEINE AND PYRILAMINE MALEATE) TABLET [RITE AID]	14
ACETAMINOPHEN	ACTIVE MOIETY	362O9ITL9D	MENSTRUAL COMPLETE MAXIMUM STRENGTH (ACETAMINOPHEN, CAFFEINE AND PYRILAMINE MALEATE) TABLET [RITE AID]	14
CAFFEINE	ACTIVE MOIETY	3G6A5W338E	MENSTRUAL COMPLETE MAXIMUM STRENGTH (ACETAMINOPHEN, CAFFEINE AND PYRILAMINE MALEATE) TABLET [RITE AID]	14
PYRILAMINE	ACTIVE MOIETY	HPE317O9TL	MENSTRUAL COMPLETE MAXIMUM STRENGTH (ACETAMINOPHEN, CAFFEINE AND PYRILAMINE MALEATE) TABLET [RITE AID]	14
CROSCARMELLOSE SODIUM	INACTIVE INGREDIENT	M28OL1HH48	MENSTRUAL COMPLETE MAXIMUM STRENGTH (ACETAMINOPHEN, CAFFEINE AND PYRILAMINE MALEATE) TABLET [RITE AID]	14
HYPROMELLOSES	INACTIVE INGREDIENT	3NXW29V3WO	MENSTRUAL COMPLETE MAXIMUM STRENGTH (ACETAMINOPHEN, CAFFEINE AND PYRILAMINE MALEATE) TABLET [RITE AID]	14
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	MENSTRUAL COMPLETE MAXIMUM STRENGTH (ACETAMINOPHEN, CAFFEINE AND PYRILAMINE MALEATE) TABLET [RITE AID]	14
POLYDEXTROSE	INACTIVE INGREDIENT	VH2XOU12IE	MENSTRUAL COMPLETE MAXIMUM STRENGTH (ACETAMINOPHEN, CAFFEINE AND PYRILAMINE MALEATE) TABLET [RITE AID]	14
POLYETHYLENE GLYCOLS	INACTIVE INGREDIENT	3WJQ0SDW1A	MENSTRUAL COMPLETE MAXIMUM STRENGTH (ACETAMINOPHEN, CAFFEINE AND PYRILAMINE MALEATE) TABLET [RITE AID]	14
STEARIC ACID	INACTIVE INGREDIENT	4ELV7Z65AP	MENSTRUAL COMPLETE MAXIMUM STRENGTH (ACETAMINOPHEN, CAFFEINE AND PYRILAMINE MALEATE) TABLET [RITE AID]	14
TITANIUM DIOXIDE	INACTIVE INGREDIENT	15FIX9V2JP	MENSTRUAL COMPLETE MAXIMUM STRENGTH (ACETAMINOPHEN, CAFFEINE AND PYRILAMINE MALEATE) TABLET [RITE AID]	14
TRIACETIN	INACTIVE INGREDIENT	XHX3C3X673	MENSTRUAL COMPLETE MAXIMUM STRENGTH (ACETAMINOPHEN, CAFFEINE AND PYRILAMINE MALEATE) TABLET [RITE AID]	14

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
11822-0390	MENSTRUAL COMPLETE MAXIMUM STRENGTH (ACETAMINOPHEN, CAFFEINE AND PYRILAMINE MALEATE) TABLET, FILM COATED [RITE AID CORPORATION]	31	Current NDC, Legacy NDC, 6 package rows	20240623_69bda7d7-8660-4e8d-b8ac-892a3b1f2124.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 9 of 79 · 1,576 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Aspirin Low Dose	ASPIRIN	ARMY AND AIR FORCE EXCHANGE SERVICE	e273ead7-7cbc-4fd5-a136-9d3558a35360	2026-06-24	Warnings	Exact identifier application number: M013
Acetaminophen Regular Strength	ACETAMINOPHEN	CVS PHARMACY	5e35df92-6282-4ca6-902b-bb6bd326b487	2026-06-23	Warnings	Exact identifier application number: M013
Pain Reliever	ACETAMINOPHEN	Orelli Inc.	4f9f1b4e-8bbb-49b9-8e6c-263edb2c084d	2026-06-22	Warnings	Exact identifier application number: M013
Pain Relief Aspirin Chewable, Low Dose	ASPIRIN	Rite Aid Corporation	65cdce0f-be04-43ba-8c68-bdce7983cfa1	2026-06-22	Warnings	Exact identifier application number: M013
Aspirin Regimen	ASPIRIN	Cardinal Health 110, LLC. DBA Leader	88f425df-712d-4911-824b-94085c7190b6	2026-06-19	Warnings	Exact identifier application number: M013
Aspirin Low Dose	ASPIRIN	Meijer Distribution, Inc.	3716a7d4-a555-4e54-aa0a-7b8f3e32addb	2026-06-19	Warnings	Exact identifier application number: M013
Pain Relief	ACETAMINOPHEN	DOLGENCORP, LLC	acc94a3e-21b6-4375-9881-38cf9bab8692	2026-06-19	Warnings	Exact identifier application number: M013
Aspirin Low Dose	ASPIRIN	L.N.K. International, Inc.	2f6ec676-3832-420e-be91-fce83f6586c8	2026-06-19	Warnings	Exact identifier application number: M013
Headache Relief	ACETAMINOPHEN, ASPIRIN, CAFFEINE	DOLGENCORP, LLC	e1e24d52-0b4d-400b-8181-e3f6ab75c4f6	2026-06-18	Warnings	Exact identifier application number: M013
Acetaminophen	ACETAMINOPHEN	Oncor Pharmaceuticals	4c396d0e-aa93-4f9e-b065-2e606f7f05cd	2026-06-17	Warnings	Exact identifier application number: M013
LOW DOSE ASPIRIN	ASPIRIN	Famora Inc.	4dc6f119-bbde-db5f-e063-6294a90a9486	2026-06-16	Warnings	Exact identifier application number: M013
Childrens Pain and Fever Relief	ACETAMINOPHEN	Chain Drug Marketing Association, Inc.	420a1e05-caa6-481f-bdab-a670f0220f96	2026-06-16	Warnings	Exact identifier application number: M013
Pain Relief Extra Strength	ACETAMINOPHEN	DOLGENCORP, LLC	ce9f4e0d-43fb-499a-b8a2-a997a14841c4	2026-06-16	Warnings	Exact identifier application number: M013
Pain Reliever	ACETAMINOPHEN	L.N.K. International, Inc.	734cc3d2-6fc5-4dcc-93ed-0b57c1f01345	2026-06-15	Warnings	Exact identifier application number: M013
RIGHT REMEDIES EXTRA STRENGTH Pain Relief PM Caplet	ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE	Strive Pharmaceuticals Inc.	2d63671d-cf7c-bbdd-e063-6294a90affef	2026-06-15	Warnings	Exact identifier application number: M013
TYLENOL Extra Strength	ACETAMINOPHEN	Kenvue Brands LLC	59773893-09a8-47a2-943a-e9ea9da4458a	2026-06-15	Warnings	Exact identifier application number: M013
Pain Relief	ACETAMINOPHEN	Shield Pharmaceuticals Corp.	96eb7f9f-ff2d-4661-bbe6-1860aafe03f6	2026-06-15	Warnings	Exact identifier application number: M013
Duralgina Extra Strength	ACETAMINOPHEN	Menper Distributors, Inc.	544e3d7e-a759-384f-e063-6294a90a5baa	2026-06-15	Warnings	Exact identifier application number: M013
pain relief childrens	ACETAMINOPHEN	Rite Aid Corporation	be2286a1-946b-4bf5-b14c-8e86da669594	2026-06-15	Warnings	Exact identifier application number: M013
Aspirin 81	ASPIRIN	Amerisource Bergen	4491faca-f30b-4eb0-bea9-f518f6b2f095	2026-06-15	Warnings	Exact identifier application number: M013

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
362O9ITL9D	ACETAMINOPHEN	103-90-2	ACETAMINOPHEN
3G6A5W338E	CAFFEINE	58-08-2	CAFFEINE
R35D29L3ZA	PYRILAMINE MALEATE	59-33-6	PYRILAMINE MALEATE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1597298	acetaminophen 500 MG / caffeine 60 MG / pyrilamine maleate 15 MG Oral Tablet	PSN	69bda7d7-8660-4e8d-b8ac-892a3b1f2124	32
1597298	acetaminophen 500 MG / caffeine 60 MG / pyrilamine maleate 15 MG Oral Tablet	SCD	69bda7d7-8660-4e8d-b8ac-892a3b1f2124	32
1597298	APAP 500 MG / Caffeine 60 MG / Pyrilamine Maleate 15 MG Oral Tablet	SY	69bda7d7-8660-4e8d-b8ac-892a3b1f2124	32

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Marketing end	Sample	Exclude flag	Status
11822-0390-1	11822039001	1 BOTTLE, PLASTIC in 1 CARTON (11822-0390-1) / 40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC	2002-04-29	2027-05-30	No	No	Current
11822-0390-8	11822039008	3 in 1 CARTON					Historical
11822-0390-9	11822039009	1 BOTTLE, PLASTIC in 1 CARTON (11822-0390-9) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC	2002-04-29	2027-05-30	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Rite Aid 44-390 MS Delisted	Rite Aid Corporation \| LNK International, Inc.	2025-06-03	HUMAN OTC DRUG LABEL	32