Low Dose Aspirin

Product NDC: 49035-563
11-digit product format: 490350563
Labeler code: 49035
Product ID: 49035-563_ea158083-c7a0-4b01-aa1d-d0e41bdc5e70
Type: HUMAN OTC DRUG
Nonproprietary name: Aspirin
Dosage form: TABLET, DELAYED RELEASE
Route: ORAL
Labeler: Wal-Mart Stores Inc
Application: M013
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2011-05-01
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
Listing certified through: 2027-12-31
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 · 2 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	49035-563	49035-563-27	D	Discontinued by firm		2026-10-12
excluded package	package	49035-563	49035-563-96	D	Discontinued by firm		2026-10-12

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 · 21 matching rows.

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

Captured / source date, Package NDC, Snapshot table
Captured / source date	Package NDC	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	49035-563-96	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	49035-563-27	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	49035-563-96	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	49035-563-27	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	49035-563-27	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	49035-563-96	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	49035-563-27	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	49035-563-96	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	49035-563-27	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	49035-563-96	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	49035-563-27	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	49035-563-96	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	49035-563-27	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	49035-563-96	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	49035-563-27	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	49035-563-96	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	49035-563-27	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	49035-563-96	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	49035-563-27	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	49035-563-27	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	49035-563-27	`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: Low Dose Aspirin
Listing expiration: 2027-12-31

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
093e0458-9975-456f-8950-8273c8890b3c	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
fb7ab793-2c12-4079-b100-a64f73bef25a	Product name	4	20240712
594e2c86-3079-4e6e-96c9-48f7a8afc78d	Product name	1	20230718
b0cbf770-6cc3-4aa4-9158-755110c2b9f7	Product name	2	20230717
dc7c5daa-021f-40dd-b00d-63982cb2067a	Product name	1	20230426
d7724692-1155-4cc8-a415-22f5fc4aec35	Product name	6	20220216
bde672ba-4805-28d0-1986-73543d41b412	Product name	2	20210201
08ffbcbf-26df-b99c-1dab-64fc4cfae89f	Product name	5	20200925
816b97af-edc5-4060-aff1-b814bdbcad50	Product name	1	20190415
7cda52fc-125f-421c-8fea-bc1974370c49	Product name	2	20180703
419aab54-5d5a-4146-9453-026d4a9991be	Product name	2	20170525
f212291f-05fe-9603-fc7e-bd73e38ce1e6	Product name	2	20161129
ade821ba-260a-47e2-bd89-743e27ac9906	Product name	1	20161121
08ffbcbf-26df-b99c-1dab-64fc4cfae89f	Product name	2	20160823
182f9ab4-4ab5-c449-200f-87ce2ce8e550	Product name	2	20151105
9425d234-4ae1-4b53-adc6-8cc7af6dd657	Product name	1	20150929
89dac932-b90a-4410-9ab1-84c53e57de25	Product name	1	20150316
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
49035-563-11	Low Dose Aspirin	60 in 1 BOTTLE, PLASTIC	TABLET, DELAYED RELEASE	60	20
49035-563-11	Low Dose Aspirin	1 in 1 CARTON	TABLET, DELAYED RELEASE	1	20
49035-563-13	Low Dose Aspirin	250 in 1 BOTTLE, PLASTIC	TABLET, DELAYED RELEASE	250	20
49035-563-13	Low Dose Aspirin	2 in 1 CARTON	TABLET, DELAYED RELEASE	2	20
49035-563-14	Low Dose Aspirin	500 in 1 BOTTLE, PLASTIC	TABLET, DELAYED RELEASE	500	20
49035-563-17	Low Dose Aspirin	300 in 1 BOTTLE, PLASTIC	TABLET, DELAYED RELEASE	300	20
49035-563-27	Low Dose Aspirin	32 in 1 BOTTLE	TABLET, DELAYED RELEASE	32	20
49035-563-27	Low Dose Aspirin	1 in 1 CARTON	TABLET, DELAYED RELEASE	1	20
49035-563-32	Low Dose Aspirin	1 in 1 CARTON	TABLET, DELAYED RELEASE	1	20
49035-563-32	Low Dose Aspirin	120 in 1 BOTTLE, PLASTIC	TABLET, DELAYED RELEASE	120	20
49035-563-96	Low Dose Aspirin	250 in 1 BOTTLE, PLASTIC	TABLET, DELAYED RELEASE	250	20
49035-563-96	Low Dose Aspirin	2 in 1 CARTON	TABLET, DELAYED RELEASE	2	20

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
49035-563-11	EA - Each	49035-563	ebec318f-1f12-41f5-a80f-930e60b07c71	1	2023-04-07
49035-563-14	EA - Each	49035-563	cd68088e-ceaf-4855-b61c-e46423863505	1	2016-03-04
49035-563-17	EA - Each	49035-563	f22db8dc-c419-4a04-98ef-288aa123113b	1	2013-02-13
49035-563-32	EA - Each	49035-563	245bd25d-686d-4f7d-80b2-d950025d4813	1	2013-10-17

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
ASPIRIN	ACTIVE INGREDIENT	R16CO5Y76E	LOW DOSE ASPIRIN (ASPIRIN) TABLET [WAL-MART STORES INC]	4
ASPIRIN	ACTIVE MOIETY	R16CO5Y76E	LOW DOSE ASPIRIN (ASPIRIN) TABLET [WAL-MART STORES INC]	4
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	LOW DOSE ASPIRIN (ASPIRIN) TABLET [WAL-MART STORES INC]	4
D&C YELLOW NO. 10	INACTIVE INGREDIENT	35SW5USQ3G	LOW DOSE ASPIRIN (ASPIRIN) TABLET [WAL-MART STORES INC]	4
HYPROMELLOSES	INACTIVE INGREDIENT	3NXW29V3WO	LOW DOSE ASPIRIN (ASPIRIN) TABLET [WAL-MART STORES INC]	4
METHACRYLIC ACID	INACTIVE INGREDIENT	1CS02G8656	LOW DOSE ASPIRIN (ASPIRIN) TABLET [WAL-MART STORES INC]	4
POLYDEXTROSE	INACTIVE INGREDIENT	VH2XOU12IE	LOW DOSE ASPIRIN (ASPIRIN) TABLET [WAL-MART STORES INC]	4
POLYETHYLENE GLYCOLS	INACTIVE INGREDIENT	3WJQ0SDW1A	LOW DOSE ASPIRIN (ASPIRIN) TABLET [WAL-MART STORES INC]	4
SHELLAC	INACTIVE INGREDIENT	46N107B71O	LOW DOSE ASPIRIN (ASPIRIN) TABLET [WAL-MART STORES INC]	4
SODIUM BICARBONATE	INACTIVE INGREDIENT	8MDF5V39QO	LOW DOSE ASPIRIN (ASPIRIN) TABLET [WAL-MART STORES INC]	4
SODIUM LAURYL SULFATE	INACTIVE INGREDIENT	368GB5141J	LOW DOSE ASPIRIN (ASPIRIN) TABLET [WAL-MART STORES INC]	4
STARCH, CORN	INACTIVE INGREDIENT	O8232NY3SJ	LOW DOSE ASPIRIN (ASPIRIN) TABLET [WAL-MART STORES INC]	4
TALC	INACTIVE INGREDIENT	7SEV7J4R1U	LOW DOSE ASPIRIN (ASPIRIN) TABLET [WAL-MART STORES INC]	4
TITANIUM DIOXIDE	INACTIVE INGREDIENT	15FIX9V2JP	LOW DOSE ASPIRIN (ASPIRIN) TABLET [WAL-MART STORES INC]	4
TRIETHYL CITRATE	INACTIVE INGREDIENT	8Z96QXD6UM	LOW DOSE ASPIRIN (ASPIRIN) TABLET [WAL-MART STORES INC]	4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
49035-563	LOW DOSE ASPIRIN (ASPIRIN) TABLET, DELAYED RELEASE [WAL-MART STORES INC]	19	Current NDC, Legacy NDC, 12 package rows	20250519_093e0458-9975-456f-8950-8273c8890b3c.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 11 of 79 · 1,579 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Childrens Mapap	ACETAMINOPHEN	Major Pharmaceuticals	efec6af2-8b26-47f6-88c8-b0a6d69a2d7d	2026-06-03	Warnings	Exact identifier application number: M013
Acetaminophen PM Extra Strength	ACETAMINOPHEN, DIPHENHYDRAMINE HCL	United Natural Foods, Inc. dba UNFI	ae3114c3-8cfe-4b81-8ac7-c281fe68b462	2026-06-03	Warnings	Exact identifier application number: M013
Acetaminophen	ACETAMINOPHEN	COSTCO WHOLESALE CORPORATION	3745aa18-a711-43ed-9bc4-1f087b3c53c0	2026-06-03	Warnings	Exact identifier application number: M013
TYLENOL Extra Strength	ACETAMINOPHEN	Kenvue Brands LLC	3f653262-b931-7d42-e063-6394a90adddd	2026-06-03	Warnings	Exact identifier application number: M013
Pain Reliever	ACETAMINOPHEN	Walgreen Company	0b1bef50-7957-4ea1-9ae3-91f59ea2dbb4	2026-06-03	Warnings	Exact identifier application number: M013
Pain Reliever PM	ACETAMINOPHEN, DIPHENHYDRAMINE HCL	WALMART INC.	42310898-cf3a-4ffb-88bb-b8b84449156e	2026-06-02	Warnings	Exact identifier application number: M013
PAIN RELIEF	ACETAMINOPHEN	Meijer, Inc.	1319bab8-8f17-44fb-9d91-099b0ba38a8d	2026-06-01	Warnings	Exact identifier application number: M013
Pain Reliever PM	ACETAMINOPHEN, DIPHENHYDRAMINE HCL	Family Dollar (FAMILY WELLNESS)	7a98d4d9-54e2-45c1-a76a-7f1907566e95	2026-06-01	Warnings	Exact identifier application number: M013
Extra Strength Acetaminophen	ACETAMINOPHEN	TIME CAP LABORATORIES, INC.	58840cf4-aceb-c7cf-e063-6294a90a5ff4	2026-06-01	Warnings	Exact identifier application number: M013
Childrens Pain and Fever	ACETAMINOPHEN	CVS Pharmacy	832acd72-1dda-4490-978f-5f31748942df	2026-06-01	Warnings	Exact identifier application number: M013
Acetaminophen PM	ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE	Major Pharmaceuticals	786dbcd5-f5c2-4491-e053-2991aa0a3437	2026-05-29	Warnings	Exact identifier application number: M013
Back and Body Extra Strength	ASPIRIN, CAFFEINE	Meijer Distribution Inc	e513f2d9-d591-4790-a117-6176ce2279dc	2026-05-29	Warnings	Exact identifier application number: M013
Chewable Acetaminophen Childrens	ACETAMINOPHEN	Cardinal Health 110, LLC. DBA Leader	5460a4b7-5da3-4fc2-a565-0b0dd11bbf44	2026-05-29	Warnings	Exact identifier application number: M013
Extra Strength Mini Softgels Pain Reliever	ACETAMINOPHEN	CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED	f55d3663-7007-41cd-ae2d-5aca6311be81	2026-05-28	Warnings	Exact identifier application number: M013
Genexa Kids Pain and Fever	ACETAMINOPHEN	Genexa Inc.	5130c695-a80e-2dd3-e063-6294a90a404f	2026-05-28	Warnings	Exact identifier application number: M013
TYLENOL Regular Strength	ACETAMINOPHEN	Kenvue Brands LLC	1622f694-4d63-4c56-8737-fae31f0ecfb7	2026-05-27	Warnings	Exact identifier application number: M013
INFANTS Pain and Fever	ACETAMINOPHEN	Aurohealth LLC	257436e1-e0f3-4a87-bffe-4f176b836caf	2026-05-27	Warnings	Exact identifier application number: M013
Infants Pain and Fever	ACETAMINOPHEN	Aurohealth LLC	6509a545-0036-460a-8f0d-b31caae17855	2026-05-27	Warnings	Exact identifier application number: M013
Alka-Seltzer Original	ANHYDROUS CITRIC ACID, ASPIRIN, AND SODIUM BICARBONATE	Select Consumer Group	3ca80d74-1e8b-49d9-e063-6394a90a4312	2026-05-24	Warnings	Exact identifier application number: M013
Pain and Fever Chewables Childrens	ACETAMINOPHEN	CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED	bad8ac0a-518d-4639-9b92-a39e0d437238	2026-05-22	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	093e0458-9975-456f-8950-8273c8890b3c	20
308416	aspirin 81 MG Delayed Release Oral Tablet	SCD	093e0458-9975-456f-8950-8273c8890b3c	20
308416	ASA 81 MG Delayed Release Oral Tablet	SY	093e0458-9975-456f-8950-8273c8890b3c	20
308416	aspirin 81 MG Enteric Coated Oral Tablet	SY	093e0458-9975-456f-8950-8273c8890b3c	20

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
49035-563-11	49035056311	1 BOTTLE, PLASTIC in 1 CARTON (49035-563-11) / 60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC		2011-05-01	0000-00-00	No	No	Current
49035-563-13	49035056313	2 BOTTLE, PLASTIC in 1 CARTON (49035-563-13) / 250 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC		2011-05-01	2027-04-30	No	No	Current
49035-563-14	49035056314	500 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (49035-563-14)		2011-05-01	0000-00-00	No	No	Current
49035-563-17	49035056317	300 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (49035-563-17)		2011-05-01	0000-00-00	No	No	Current
49035-563-27	49035056327	1 BOTTLE in 1 CARTON (49035-563-27) > 32 TABLET in 1 BOTTLE	1 bottle	2011-05-01	0000-00-00	No	No	Current
49035-563-32	49035056332	1 BOTTLE, PLASTIC in 1 CARTON (49035-563-32) / 120 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC		2011-05-01	0000-00-00	No	No	Current
49035-563-96	49035056396	2 BOTTLE in 1 CARTON (49035-563-96) > 250 TABLET in 1 BOTTLE	2 bottle	2011-05-01	0000-00-00	No	No	Current