FDA.reportPublic FDA data

Acetaminophen - Hi-Tech Nutraceuticals, LLC

Manufacturer
Hi-Tech Nutraceuticals, LLC
Effective date
2026-07-06
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
weekly-update
Hydrated at
2026-07-17 21:43:38

Label at a glance#

ProductAcetaminophen
Active ingredientACETAMINOPHEN
Label structure17 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 Doc or PharmAsk a Doc or Pharm

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

PregnancyPregnancy

OTC - PURPOSE SECTION

PurposePurpose

OTC - QUESTIONS SECTION

QuestionsQuestions

OTC - STOP USE SECTION

Stop UseStop Use

OTC - WHEN USING SECTION

Directions when usingDirections when using

OVERDOSAGE SECTION

OverdoseOverdose

WARNINGS SECTION

WarningsWarnings

INDICATIONS & USAGE SECTION

UsesUses

INACTIVE INGREDIENT SECTION

InactivesInactives

STORAGE AND HANDLING SECTION

Storage and HandlingStorage and Handling

DOSAGE & ADMINISTRATION SECTION

DirectionsDirections

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PDPPDP

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69732-002-012024-01-30C16284748780-11030e365-59be-111a-e063-dadaa90a10e2a39c524e-c131-d7fb-e053-2995a90a785b
69732-002-012024-01-30C16284748780-11030e365-59be-111a-e063-dadaa90a10e2a39c524e-c131-d7fb-e053-2995a90a785b

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
69732-00269732-002-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
SODIUM STARCH GLYCOLATE TYPE AH8AV0SQX4DIACT
MAGNESIUM STEARATE70097M6I30IACT
HYPROMELLOSE, UNSPECIFIED3NXW29V3WOIACT
ACETAMINOPHEN362O9ITL9DACTIB

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
32022-12-31full-release2026-05-31 23:52:49

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
AcetaminophenACETAMINOPHENHi-Tech Nutraceuticals, LLCa39c524e-c131-d7fb-e053-2995a90a785b2026-07-06WarningsExact identifier
ndc (package): 69732-002-01
ndc (product): 69732-002
ndc11 (package): 69732000201
spl id: 55f942de-2c2c-8d1c-e063-6394a90aa7a8
spl set id: a39c524e-c131-d7fb-e053-2995a90a785b

Reported adverse events (FAERS/openFDA)#

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