FDA.reportPublic FDA data

Extra Strength Pain Reliever

Manufacturer
PuraCap Pharmaceutical LLC | Humanwell PuraCap Pharmaceutical (Wuhan) Co., Ltd.
Effective date
2019-11-25
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:01:41

Label at a glance#

ProductExtra Strength Pain Reliever
Active ingredientACETAMINOPHEN
Label structure12 sections

Indications and uses

temporarily relieves minor aches and pains due to: the common cold headache backache minor pain of arthritis toothache muscular aches premenstrual and menstrual cramps temporarily reduces fever

Dosage and administration

do not take more than directed (see Overdose warning) adults and children 12 years and over take 2 softgels every 6 hours while symptoms last do not take more than 6 softgels in 24 hours, unless directed by a doctor do not use for more than 10 days unless directed by a doctor children under 12 years ask a doctor

Storage and handling

store at room temperature 15°-30°C (59°-86°F)

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient (in each softgel)

OTC - ACTIVE INGREDIENT SECTION

Acetaminophen 500 mg

Purpose

OTC - PURPOSE SECTION

Pain reliever/fever reducer

Uses

INDICATIONS & USAGE SECTION

  • temporarily relieves minor aches and pains due to:
    • the common cold
    • headache
    • backache
    • minor pain of arthritis
    • toothache
    • muscular aches
    • premenstrual and menstrual cramps
  • temporarily reduces fever

Warnings

WARNINGS SECTION

Liver warning: This product contains acetaminophen. Severe liver damage may occur if you take

  • more than 4,000 mg of acetaminophen in 24 hours
  • with other drugs containing acetaminophen
  • 3 or more alcoholic drinks every day while using this product

Allergy alert: Acetaminophen may cause severe skin reactions. Symptoms may include:

  • skin reddening
  • blisters
  • rash

If a skin reaction occurs, stop use and seek medical help right away.

Do not use

OTC - DO NOT USE SECTION

  • with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist
  • if you are allergic to acetaminophen or any of the inactive ingredients in this product

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have liver disease

OTC - ASK DOCTOR/PHARMACIST SECTION

Ask a doctor or pharmacist before use if you are taking the blood thinning drug warfarin

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • pain gets worse or lasts more than 10 days
  • fever gets worse or lasts more than 3 days
  • new symptoms occur
  • redness or swelling is present

These could be signs of a serious condition.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Overdose warning

OVERDOSAGE SECTION

In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222). Quick medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.

Directions

DOSAGE & ADMINISTRATION SECTION

  • do not take more than directed (see Overdose warning)

adults and children 12 years and over

  • take 2 softgels every 6 hours while symptoms last
  • do not take more than 6 softgels in 24 hours, unless directed by a doctor
  • do not use for more than 10 days unless directed by a doctor

children under 12 years

ask a doctor

Other information

STORAGE AND HANDLING SECTION

  • store at room temperature 15°-30°C (59°-86°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

FD&C red #40, FD&C yellow #6, gelatin, glycerin, polyethylene glycol, povidone, propylene glycol, purified water, sorbitol sorbitan solution and white edible ink

Questions or Comments?

OTC - QUESTIONS SECTION

Call : 1-888-309-9030

PRINCIPAL DISPLAY PANEL - Bottle Label 20ct

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DG Extra Strength Pain Reliever 20 Softgels

Acetaminophen 500mg

NDC 51013-172-15

*Compare to the active ingredient in TYLENOL® Extra Strength

Bottle Label 20ct FrontBottle Label 20ct Front

Bottle Label 20ct BackBottle Label 20ct Back

PRINCIPAL DISPLAY PANEL - Bottle Label 40ct

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DG Extra Strength Pain Reliever 40 Softgels

Acetaminophen 500mg

NDC 51013-172-25

*Compare to the active ingredient in TYLENOL® Extra Strength

Bottle Label 40ct FrontBottle Label 40ct Front

Bottle Label 40ct BackBottle Label 40ct Back

PRINCIPAL DISPLAY PANEL - Bottle Label 24ct

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DG Extra Strength Pain Reliever 24 Softgels

Acetaminophen 500mg

NDC 51013-172-43

*Compare to the active ingredient in TYLENOL® Extra Strength

Bottle Label 24ct FrontBottle Label 24ct Front

Bottle Label 24ct BackBottle Label 24ct Back

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
198439acetaminophen 500 MG Oral CapsulePSN3
198439acetaminophen 500 MG Oral CapsuleSCD3
198439APAP 500 MG Oral CapsuleSY3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51013-172-152025-01-30C16284748780-12cef2736-b411-d83d-e063-dadaa90ab31fExtra Strength Pain Reliever
51013-172-252025-01-30C16284748780-12cef2736-b411-d83d-e063-dadaa90ab31fExtra Strength Pain Reliever
51013-172-432025-01-30C16284748780-12cef2736-b411-d83d-e063-dadaa90ab31fExtra Strength Pain Reliever

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51013-172-15Extra Strength Pain Reliever20 in 1 BOTTLECAPSULE, LIQUID FILLED203
51013-172-25Extra Strength Pain Reliever40 in 1 BOTTLECAPSULE, LIQUID FILLED403
51013-172-43Extra Strength Pain Reliever24 in 1 BOTTLECAPSULE, LIQUID FILLED243

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51013-172EXTRA STRENGTH PAIN RELIEVER (ACETAMINOPHEN) CAPSULE, LIQUID FILLED [PURACAP PHARMACEUTICAL LLC]3Legacy NDC, 3 package rows20191126_7aae8651-d4ba-46e8-82e1-28bee0f66caa.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51013-17251013-172-15, 51013-172-25, 51013-172-43

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
ACETAMINOPHEN362O9ITL9DACTIB
FD&C RED NO. 40WZB9127XOAIACT
FD&C YELLOW NO. 6H77VEI93A8IACT
GELATIN2G86QN327LIACT
GLYCERINPDC6A3C0OXIACT
POLYETHYLENE GLYCOL, UNSPECIFIED3WJQ0SDW1AIACT
POVIDONEFZ989GH94EIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
WATER059QF0KO0RIACT
SORBITOL506T60A25RIACT
SORBITAN6O92ICV9RUIACT

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
ac5ea99e-f61c-4e77-af52-28c527448b037aae8651-d4ba-46e8-82e1-28bee0f66caa2019-11-25WarningsExact identifier
spl id: ac5ea99e-f61c-4e77-af52-28c527448b03
spl set id: 7aae8651-d4ba-46e8-82e1-28bee0f66caa

Reported adverse events (FAERS/openFDA)#

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