Aspirin 81 mg

Product NDC: 41250-600
11-digit product format: 412500600
Labeler code: 41250
Product ID: 41250-600_2356853e-64a8-4fa9-87db-a77f3277fb6c
Type: HUMAN OTC DRUG
Nonproprietary name: Aspirin
Dosage form: TABLET, DELAYED RELEASE
Route: ORAL
Labeler: Meijer Distribution Inc
Application: M013
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2011-05-01
Marketing end: 2026-11-02
Substance: ASPIRIN
Active strength: 81 mg/1
Pharmacologic classes: Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Decreased Platelet Aggregation [PE], Decreased Prostaglandin Production [PE], Nonsteroidal Anti-inflammatory Drug [EPC], Platelet Aggregation Inhibitor [EPC]
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	41250-600	41250-600-32	D	Discontinued by firm		2026-10-05

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: Aspirin 81 mg
Brand name suffix: Low Dose

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
ASPIRIN	81 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
R16CO5Y76E	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
308416	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
eb29d6be-f095-44b2-b6ed-7e4167b596f8	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
d7724692-1155-4cc8-a415-22f5fc4aec35	Product name	6	20220216
bde672ba-4805-28d0-1986-73543d41b412	Product name	2	20210201
f212291f-05fe-9603-fc7e-bd73e38ce1e6	Product name	2	20161129
ade821ba-260a-47e2-bd89-743e27ac9906	Product name	1	20161121
182f9ab4-4ab5-c449-200f-87ce2ce8e550	Product name	2	20151105
9425d234-4ae1-4b53-adc6-8cc7af6dd657	Product name	1	20150929
2a21311a-89e2-0e83-2ebd-117f9798b2b2	Product name	1	20140508
9007e8a7-ff50-f9b9-7945-f2a1deadd94e	Product name	1	20140508
96c2be53-8e44-452d-56a2-d255b2f1af2d	Product name	1	20140508
bf8bd5f7-495f-4022-2780-7ded7ea7ea44	Product name	1	20140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
41250-600-14	Aspirin 81 mgLow Dose	500 in 1 BOTTLE, PLASTIC	TABLET, DELAYED RELEASE	500	14
41250-600-32	Aspirin 81 mgLow Dose	1 in 1 CARTON	TABLET, DELAYED RELEASE	1	14
41250-600-32	Aspirin 81 mgLow Dose	120 in 1 BOTTLE	TABLET, DELAYED RELEASE	120	14
41250-600-98	Aspirin 81 mgLow Dose	2 in 1 CARTON	TABLET, DELAYED RELEASE	2	14
41250-600-98	Aspirin 81 mgLow Dose	365 in 1 BOTTLE, PLASTIC	TABLET, DELAYED RELEASE	365	14

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
ASPIRIN	ACTIVE INGREDIENT	R16CO5Y76E	ASPIRIN 81 MG LOW DOSE (ASPIRIN) TABLET, COATED [MEIJER]	1
ASPIRIN	ACTIVE MOIETY	R16CO5Y76E	ASPIRIN 81 MG LOW DOSE (ASPIRIN) TABLET, COATED [MEIJER]	1
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	ASPIRIN 81 MG LOW DOSE (ASPIRIN) TABLET, COATED [MEIJER]	1
D&C YELLOW NO. 10	INACTIVE INGREDIENT	35SW5USQ3G	ASPIRIN 81 MG LOW DOSE (ASPIRIN) TABLET, COATED [MEIJER]	1
FD&C YELLOW NO. 6	INACTIVE INGREDIENT	H77VEI93A8	ASPIRIN 81 MG LOW DOSE (ASPIRIN) TABLET, COATED [MEIJER]	1
HYPROMELLOSES	INACTIVE INGREDIENT	3NXW29V3WO	ASPIRIN 81 MG LOW DOSE (ASPIRIN) TABLET, COATED [MEIJER]	1
METHACRYLIC ACID	INACTIVE INGREDIENT	1CS02G8656	ASPIRIN 81 MG LOW DOSE (ASPIRIN) TABLET, COATED [MEIJER]	1
POLYDEXTROSE	INACTIVE INGREDIENT	VH2XOU12IE	ASPIRIN 81 MG LOW DOSE (ASPIRIN) TABLET, COATED [MEIJER]	1
POLYETHYLENE GLYCOLS	INACTIVE INGREDIENT	3WJQ0SDW1A	ASPIRIN 81 MG LOW DOSE (ASPIRIN) TABLET, COATED [MEIJER]	1
SODIUM BICARBONATE	INACTIVE INGREDIENT	8MDF5V39QO	ASPIRIN 81 MG LOW DOSE (ASPIRIN) TABLET, COATED [MEIJER]	1
SODIUM LAURYL SULFATE	INACTIVE INGREDIENT	368GB5141J	ASPIRIN 81 MG LOW DOSE (ASPIRIN) TABLET, COATED [MEIJER]	1
STARCH, CORN	INACTIVE INGREDIENT	O8232NY3SJ	ASPIRIN 81 MG LOW DOSE (ASPIRIN) TABLET, COATED [MEIJER]	1
TALC	INACTIVE INGREDIENT	7SEV7J4R1U	ASPIRIN 81 MG LOW DOSE (ASPIRIN) TABLET, COATED [MEIJER]	1
TITANIUM DIOXIDE	INACTIVE INGREDIENT	15FIX9V2JP	ASPIRIN 81 MG LOW DOSE (ASPIRIN) TABLET, COATED [MEIJER]	1
TRIACETIN	INACTIVE INGREDIENT	XHX3C3X673	ASPIRIN 81 MG LOW DOSE (ASPIRIN) TABLET, COATED [MEIJER]	1
TRIETHYL CITRATE	INACTIVE INGREDIENT	8Z96QXD6UM	ASPIRIN 81 MG LOW DOSE (ASPIRIN) TABLET, COATED [MEIJER]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
41250-600	ASPIRIN 81 MG LOW DOSE (ASPIRIN) TABLET, DELAYED RELEASE [MEIJER DISTRIBUTION INC]	14	Current NDC, Legacy NDC, 5 package rows	20250104_eb29d6be-f095-44b2-b6ed-7e4167b596f8.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 4 of 83 · 1,657 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
pain relief childrens	ACETAMINOPHEN	Rite Aid Corporation	29ecdd2d-aeaf-40a8-a347-011088009ea6	2026-08-11	Warnings	Exact identifier application number: M013
Fast Acting Pedia Crae	ACETAMINOPHEN	Randob Labs., Ltd.	e069060f-fbb2-4c7a-b872-00b3ab86d01b	2026-08-11	Warnings	Exact identifier application number: M013
ASPIRIN	ASPIRIN	Amazon.com Services LLC	c7cc0681-4c0b-4565-99df-d0168c8ba1ba	2026-08-10	Warnings	Exact identifier application number: M013
GenCare Headache Relief	ACETAMINOPHEN, ASPIRIN, CAFFEINE	Pioneer Life Sciences, LLC	ac8c4bdf-30c9-2b09-e053-2a95a90a9b67	2026-08-09	Warnings	Exact identifier application number: M013
Gencare-Aspirin Low Dose Pain reliever (NSAID)	ASPIRIN	Pioneer Life Sciences, LLC	24d4f46a-c7a5-4e94-804f-1e307d8e8cfc	2026-08-09	Warnings	Exact identifier application number: M013
Aspirin 81 mg	ASPIRIN	DOLGENCORP, LLC	b4064039-2345-4227-b83d-54dc13a838d3	2026-08-07	Warnings	Exact identifier application number: M013
Aspirin Low Dose	ASPIRIN	United Natural Foods, Inc. dba UNFI	87def9e0-0246-42cf-b8ea-2513d52e9f68	2026-08-07	Warnings	Exact identifier application number: M013
berkley and jensen acetaminophen	ACETAMINOPHEN	BJWC	dee57d73-73ac-48bb-b1da-9971f1ff21c4	2026-08-07	Warnings	Exact identifier application number: M013
Pain Reliever PM Extra Strength	ACETAMINOPHEN, DIPHENHYDRAMINE HCL	Salado Sales, Inc.	aef30709-f33d-48ff-b2d4-0639ffbd1ffd	2026-08-07	Warnings	Exact identifier application number: M013
Aspirin	ASPIRIN	P & L Development, LLC	4cd74cec-a209-4e92-b853-fbe5c95f7678	2026-08-06	Warnings	Exact identifier application number: M013
Tension Headache Aspirin-Free	ACETAMINOPHEN, CAFFEINE	Rite Aid Corporation	093a7c26-f2b1-4416-b193-81133d247d2e	2026-08-06	Warnings	Exact identifier application number: M013
ACETAMINOPHEN	ACETAMINOPHEN	Kroger Company	bc17b2e5-4828-6a2e-e053-2995a90a8c63	2026-08-05	Warnings	Exact identifier application number: M013
Infants TYLENOL	ACETAMINOPHEN	Kenvue Brands LLC	997b9551-c222-4a9c-8ba1-09a5f97495fa	2026-08-05	Warnings	Exact identifier application number: M013
Mantra Pain Gel raspberry	ACETAMINOPHEN	MOREMED INC.	7c8bdf49-a6d2-4e42-b006-375f103fd0ac	2026-08-05	Warnings	Exact identifier application number: M013
Acetaminophen	ACETAMINOPHEN	HARRIS TEETER	d2d2846d-4e0b-4d42-b300-60dd3b2cca1b	2026-08-05	Warnings	Exact identifier application number: M013
Acetaminophen	ACETAMINOPHEN	HARRIS TEETER	960f5676-d8c5-470b-a663-4b8d152339b4	2026-08-05	Warnings	Exact identifier application number: M013
Acetaminophen	ACETAMINOPHEN	HARRIS TEETER	a60f6439-2033-4bd2-b78c-6c083414a12b	2026-08-05	Warnings	Exact identifier application number: M013
pain relief PM	ACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE	HARRIS TEETER	0afb6181-d0b1-4845-8230-faabf1b997dc	2026-08-05	Warnings	Exact identifier application number: M013
Acetaminophen PM	ACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE	Harris Teeter	8a3e3439-90ae-4fc9-8ff2-44b8363fa338	2026-08-05	Warnings	Exact identifier application number: M013
Acetaminophen	ACETAMINOPHEN	Harris Teeter	50e7b939-e0eb-44ea-82ea-034e844e2c29	2026-08-05	Warnings	Exact identifier application number: M013

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
R16CO5Y76E	ASPIRIN	50-78-2	ASPIRIN

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
308416	aspirin 81 MG Delayed Release Oral Tablet	PSN	eb29d6be-f095-44b2-b6ed-7e4167b596f8	14
308416	aspirin 81 MG Delayed Release Oral Tablet	SCD	eb29d6be-f095-44b2-b6ed-7e4167b596f8	14
308416	ASA 81 MG Delayed Release Oral Tablet	SY	eb29d6be-f095-44b2-b6ed-7e4167b596f8	14
308416	aspirin 81 MG Enteric Coated Oral Tablet	SY	eb29d6be-f095-44b2-b6ed-7e4167b596f8	14

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Marketing end	Sample	Exclude flag	Status
41250-600-14	41250060014	500 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (41250-600-14)	2011-05-01	2026-11-02	No	No	Current
41250-600-32	41250060032	1 in 1 CARTON					Historical
41250-600-98	41250060098	2 BOTTLE, PLASTIC in 1 CARTON (41250-600-98) / 365 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC	2011-05-01	2026-11-02	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Meijer 44-600A-Delisted	Meijer Distribution Inc \| LNK International, Inc.	2025-01-02	HUMAN OTC DRUG LABEL	14