Aspirin

Product NDC: 17714-121
11-digit product format: 177140121
Labeler code: 17714
Product ID: 17714-121_5cc8bd8c-1d8c-180b-e053-2a91aa0ac490
Type: HUMAN OTC DRUG
Nonproprietary name: Aspirin
Dosage form: TABLET
Route: ORAL
Labeler: Advance Pharmaceutical Inc.
Application: part343
Marketing category: OTC MONOGRAPH FINAL
Marketing start: 1999-06-12
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: 2026-12-31
Current FDA listing: Yes

Additional Listing Data#

Finished product: Yes
Brand name base: Aspirin
Listing expiration: 2026-12-31

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
8977b821-2843-4436-bd3b-bb902a4b787e	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
17714-121-06	Aspirin	240 in 1 BOTTLE	TABLET	240	3
17714-121-10	Aspirin	1000 in 1 BOTTLE	TABLET	1000	3
17714-121-12	Aspirin	120 in 1 BOTTLE	TABLET	120	3

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
ASPIRIN	ACTIVE INGREDIENT	R16CO5Y76E	ASPIRIN TABLET [ADVANCE PHARMACEUTICAL INC.]	2
ASPIRIN	ACTIVE MOIETY	R16CO5Y76E	ASPIRIN TABLET [ADVANCE PHARMACEUTICAL INC.]	2
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	ASPIRIN TABLET [ADVANCE PHARMACEUTICAL INC.]	2
CROSCARMELLOSE SODIUM	INACTIVE INGREDIENT	M28OL1HH48	ASPIRIN TABLET [ADVANCE PHARMACEUTICAL INC.]	2
D&C YELLOW NO. 10	INACTIVE INGREDIENT	35SW5USQ3G	ASPIRIN TABLET [ADVANCE PHARMACEUTICAL INC.]	2
HYPROMELLOSES	INACTIVE INGREDIENT	3NXW29V3WO	ASPIRIN TABLET [ADVANCE PHARMACEUTICAL INC.]	2
METHACRYLIC ACID	INACTIVE INGREDIENT	1CS02G8656	ASPIRIN TABLET [ADVANCE PHARMACEUTICAL INC.]	2
POLYETHYLENE GLYCOL 1000	INACTIVE INGREDIENT	U076Q6Q621	ASPIRIN TABLET [ADVANCE PHARMACEUTICAL INC.]	2
POVIDONE	INACTIVE INGREDIENT	FZ989GH94E	ASPIRIN TABLET [ADVANCE PHARMACEUTICAL INC.]	2
PROPYLENE GLYCOL	INACTIVE INGREDIENT	6DC9Q167V3	ASPIRIN TABLET [ADVANCE PHARMACEUTICAL INC.]	2
SILICON DIOXIDE	INACTIVE INGREDIENT	ETJ7Z6XBU4	ASPIRIN TABLET [ADVANCE PHARMACEUTICAL INC.]	2
SODIUM LAURYL SULFATE	INACTIVE INGREDIENT	368GB5141J	ASPIRIN TABLET [ADVANCE PHARMACEUTICAL INC.]	2
STARCH, CORN	INACTIVE INGREDIENT	O8232NY3SJ	ASPIRIN TABLET [ADVANCE PHARMACEUTICAL INC.]	2
STEARIC ACID	INACTIVE INGREDIENT	4ELV7Z65AP	ASPIRIN TABLET [ADVANCE PHARMACEUTICAL INC.]	2
TALC	INACTIVE INGREDIENT	7SEV7J4R1U	ASPIRIN TABLET [ADVANCE PHARMACEUTICAL INC.]	2
TITANIUM DIOXIDE	INACTIVE INGREDIENT	15FIX9V2JP	ASPIRIN TABLET [ADVANCE PHARMACEUTICAL INC.]	2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
17714-121	ASPIRIN TABLET [ADVANCE PHARMACEUTICAL INC.]	3	Current NDC, Legacy NDC, 3 package rows	20171031_8977b821-2843-4436-bd3b-bb902a4b787e.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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Aspirin	ASPIRIN	Advance Pharmaceutical Inc.	8977b821-2843-4436-bd3b-bb902a4b787e	2017-10-30	Warnings	Exact identifier ndc (product): 17714-121

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	8977b821-2843-4436-bd3b-bb902a4b787e	3
308416	aspirin 81 MG Delayed Release Oral Tablet	SCD	8977b821-2843-4436-bd3b-bb902a4b787e	3
308416	ASA 81 MG Delayed Release Oral Tablet	SY	8977b821-2843-4436-bd3b-bb902a4b787e	3
308416	aspirin 81 MG Enteric Coated Oral Tablet	SY	8977b821-2843-4436-bd3b-bb902a4b787e	3

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
17714-121-06	17714012106	240 TABLET in 1 BOTTLE (17714-121-06)	240 tablet	2013-05-01	0000-00-00	No	No	Current
17714-121-10	17714012110	1000 TABLET in 1 BOTTLE (17714-121-10)	1000 tablet	2015-08-01	0000-00-00	No	No	Current
17714-121-12	17714012112	120 TABLET in 1 BOTTLE (17714-121-12)	120 tablet	2013-05-01	0000-00-00	No	No	Current