EXTRA STRENGTH HEADACHE RELIEF

Manufacturer
TARGET CORPORATION | TIME CAP LABORATORIES, INC | TIME CAP LABORATORIES, INC.
Effective date
2019-09-18
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:47:13

Label at a glance#

ProductEXTRA STRENGTH HEADACHE RELIEF
Active ingredientCAFFEINE, ACETAMINOPHEN, ASPIRIN
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ACETAMINOPHEN 250 MG - ASPIRIN 250 MG (nsaid*) CAFFEINE 65 MG - * NONSTEROIDAL ANIT-INFLAMMATORY DRUG

INACTIVE INGREDIENT SECTION

STEARIC ACID
MINERAL OIL
SILICON DIOXIDE
HYPROMELLOSES

MICROCRYSTALLINE CELLULOSE
STARCH, CORN
POVIDONE
CARNAUBA WAX

TITANIUM DIOXIDE
SODIUM STARCH GLYCOLATE

OTC - PURPOSE SECTION

PURPOSE

PAIN RELIEVER - PAIN RELIEVER AID

INDICATIONS & USAGE SECTION

TEMPORARILY RELIEVES MINOR ACHES AND PAINS DUE TO: headache - a cold - arthritis - muscular aches - toothache - premenstrual and menstrual cramps

DOSAGE & ADMINISTRATION SECTION

DO NOT USE MORE THAN DIRECTED - DRINK A FULL GLASS OF WATER WITH EACH DOSE - ADULTS AND CHILDREN 12 YEARS AND OVER: TAKE 2 CAPLETS EVERY 6 HOURS, NOT MORE THAN 8 CAPLETS IN 24 HOURS.
CHILDREN UNDER 12 YEARS: ASK A DOCTOR

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

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

WARNINGS SECTION

WARNINGS

REYE'S SYNDROME:

Children and teenagers who have or are recovering from chickenpox or flu-like symptoms should not use this product. When using this product, if changes in behavior with nausea and vomiting occur, consult a doctor because these symptoms could be an early sign of Reye's syndrome, a rare but serious illness.

ALLERGY ALERT

Aspirin may cause a severe allergic reaction which may include:

hives

facial swelling

asthma (sneezing)

shock

LIVER WARNING:

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

more than 8 caplets in 24 hours, which is the maximum daily amount;

with other drugs containing acetaminophen;

3 or more alcoholic drinks every day while using this product

STOMACH BLEEDING WARNING:

This product contains an NSAID, which may cause severe stomach bleeding. The chance is higher if you:

are age 60 or older;

have had stomach ulcers or bleeding problems

take a blood-thinning (anticoagulant) or steroid drug

take other drugs containing prescription or nonprescription NSAIDs (aspirin, ibuprofen, naproxen, or others)

take more or for a longer time than directed

CAFFEINE WARNING:

The recommended dose of this product contains about as much caffeine as a cup of coffee. Limit the use of caffeine-containing medications, foods or beverages which while taking this product because too much caffeine may cause nervousness, irritability, sleeplessness and occasionally, rapid heartbeat.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

100CT NDC 305100CT NDC 305

FDA-Initiated Inactive NDC Indexing#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11673-305EXTRA STRENGTH HEADACHE RELIEF (ACETAMINOPHEN-ASPIRIN-CAFFEINE) TABLET, COATED [TARGET CORPORATION]2Legacy NDC20200101_8e878f9f-e692-c140-e053-2995a90a5242.zip

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
11673-30511673-305-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 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
47258e06-b884-b2cd-e063-6394a90a64fd8e878f9f-e692-c140-e053-2995a90a52422025-12-30WarningsExact identifier
spl set id: 8e878f9f-e692-c140-e053-2995a90a5242

Reported adverse events (FAERS/openFDA)#

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