Acetaminophen Caplets

Product NDC: 70729-175
Requested package NDC: 70729-175-12
11-digit product format: 707290175
Labeler code: 70729
Product ID: 70729-175_62ddc12d-7480-4db8-a784-e2e1503fad2b
Type: HUMAN OTC DRUG
Nonproprietary name: Acetaminophen
Dosage form: TABLET
Route: ORAL
Labeler: Breeden Brothers, LLC
Application: part343
Marketing category: OTC MONOGRAPH NOT FINAL
Marketing start: 2017-05-01
Substance: ACETAMINOPHEN
Active strength: 500 mg/1
NDC exclude flag: No
Listing certified through: 2026-12-31
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: Acetaminophen Caplets
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
ACETAMINOPHEN	500 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
362O9ITL9D	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
198440	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
57fff3dc-ba30-4d3d-9362-01df6974f813	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
70729-175-12	Acetaminophen Caplets	100 in 1 BOTTLE, PLASTIC	TABLET	100		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
70729-175	ACETAMINOPHEN CAPLETS (ACETAMINOPHEN) TABLET [BREEDEN BROTHERS, LLC]	2	Current NDC, Legacy NDC, 1 package rows	20180929_57fff3dc-ba30-4d3d-9362-01df6974f813.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
Acetaminophen Caplets	ACETAMINOPHEN	Breeden Brothers, LLC	57fff3dc-ba30-4d3d-9362-01df6974f813	2017-02-15	Warnings	Exact identifier ndc (package): 70729-175-12 ndc (product): 70729-175 ndc11 (package): 70729017512

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
362O9ITL9D	ACETAMINOPHEN	103-90-2	ACETAMINOPHEN

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
198440	acetaminophen 500 MG Oral Tablet	PSN	57fff3dc-ba30-4d3d-9362-01df6974f813	2
198440	acetaminophen 500 MG Oral Tablet	SCD	57fff3dc-ba30-4d3d-9362-01df6974f813	2
198440	APAP 500 MG Oral Tablet	SY	57fff3dc-ba30-4d3d-9362-01df6974f813	2

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
70729-175-12	70729017512	100 TABLET in 1 BOTTLE, PLASTIC (70729-175-12)	100 tablet	2017-05-01	0000-00-00	No	No	Current