Aspirin 325 mg

Manufacturer
Hi-Tech Nutraceuticals, LLC
Effective date
2026-07-01
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
weekly-update
Hydrated at
2026-07-17 21:43:32

Label at a glance#

ProductAspirin 325 mg
Active ingredientASPIRIN
Label structure16 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ActivesActives

OTC - ASK DOCTOR SECTION

Ask a DoctorAsk a Doctor

OTC - ASK DOCTOR/PHARMACIST SECTION

Ask a D or PAsk a D or P

OTC - DO NOT USE SECTION

Do Not UseDo Not Use

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of childrenKeep out of reach of children

OTC - PREGNANCY OR BREAST FEEDING SECTION

if P or Bif P or B

OTC - PURPOSE SECTION

PurposesPurposes

OTC - QUESTIONS SECTION

QuestionsQuestions

OTC - STOP USE SECTION

Stop UseStop Use

OTC - WHEN USING SECTION

When UsingWhen Using

OVERDOSAGE SECTION

OverdosageOverdosage

DOSAGE & ADMINISTRATION SECTION

Dosage and AdministrationDosage and Administration

WARNINGS SECTION

WarningsWarnings

INDICATIONS & USAGE SECTION

UsesUses

INACTIVE INGREDIENT SECTION

InactivesInactives

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PDPPDP

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69732-00869732-008-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Source Document#

Source XML

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Aspirin 325 mgASPIRINHi-Tech Nutraceuticals, LLCb3426a9a-ea99-da30-e053-2995a90a1e4b2026-07-01WarningsExact identifier
ndc (package): 69732-008-01
ndc (product): 69732-008
ndc11 (package): 69732000801
spl id: b70135a1-c94a-14e1-e053-2995a90a55b4
spl set id: b3426a9a-ea99-da30-e053-2995a90a1e4b

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.