Sunmark Arthritis Pain Reliever

Manufacturer
Sunmark | Ohm Laboratories Inc.
Effective date
2012-08-16
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:32:49

Key Label Information

Active Ingredients And Purpose

ACTIVE INGREDIENT (IN EACH CAPLET)

Acetaminophen USP, 650 mg

PURPOSE

Pain reliever/fever reducer

Uses

USES

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

Warnings

WARNINGS

Liver warning: This product contains acetaminophen. Severe liver damage may occur if you take more than 6 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

Directions And Dosage

DIRECTIONS

do not take more than directed (see overdose warning) Adults take 2 caplets every 8 hours with water swallow whole - do not crush, chew, split or dissolve do not take more than 6 caplets in 24 hours do not use for more than 10 days unless directed by a doctor under 18 years of age ask a doctor

Other Label Information

INACTIVE INGREDIENTS

croscarmellose sodium, hypromellose, magnesium stearate, microcrystalline cellulose, povidone, pregelatinized starch, propylene glycol, sodium lauryl sulfate, stearic acid, titanium dioxide

QUESTIONS?

call 1-800-406-7984 Keep the carton. It contains important information. Contains No Aspirin. Distributed By McKesson One Post Street, San Francisco, CA 94104 www.sunmarkbrand.com

PRINCIPAL DISPLAY PANEL

sunmark ® NDC 49348-921-09 See New Warnings Information arthritis pain relief Acetaminophen Extended-Release Tablets, USP 650 mg Pain Reliever/Fever Reducer For the Temporary Relief of Minor Arthritis Pain LASTS UP TO 8 HOURS Use only as directed. 50 CAPLETS * 650 mg EACH ( * capsule-shaped tablets) DO NOT USE WITH OTHER MEDICINES CONTAINING ACETAMINOPHEN COMPARE TO TYLENOL ® ARTHRITIS PAIN ACTIVE INGREDIENT † † This product is not manufactured or distributed by McNeil Consumer Healthcare, Inc. The owner of the registered trademark Tylenol ® is The Tylenol Company. sunmark ® NDC 49348-921-10 See New Warnings Information arthritis pain relief Acetaminophen Extended-Release Tablets, USP 650 mg Pain Reliever/Fever Reducer For the Temporary Relief of Minor Arthritis Pain LASTS UP TO 8 HOURS Use only as directed. 100 CAPLETS * 650 mg EACH ( * capsule-shaped tablets) THIS PACKAGE FOR HOUSEHOLDS WITHOUT YOUNG CHILDREN EASY TO OPEN BOTTLE DO NOT USE WITH OTHER MEDICINES CONTAINING ACETAMINOPHEN COMPARE TO TYLENOL ® ARTHRITIS PAIN ACTIVE INGREDIENT † † This product is not manufactured or distributed by McNeil Consumer Healthcare, Inc. The owner of the registered trademark Tylenol ® is The Tylenol Company.

Label Images

APAPArthritis
APAPArthritis
APAP-100
APAP-100

Products

NDC Codes

Ingredients

Complete SPL Sections

ACTIVE INGREDIENT (IN EACH CAPLET)

OTC - ACTIVE INGREDIENT SECTION

Acetaminophen USP, 650 mg

PURPOSE

OTC - PURPOSE SECTION

Pain reliever/fever reducer

USES

INDICATIONS & USAGE SECTION

temporarily relieves minor aches and pains due to: minor pain of arthritis muscular aches backache headache toothache the common cold 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 6 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

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

do not take more than directed (see overdose warning) Adults take 2 caplets every 8 hours with water swallow whole - do not crush, chew, split or dissolve do not take more than 6 caplets in 24 hours do not use for more than 10 days unless directed by a doctor under 18 years of age ask a doctor

OTHER INFORMATION

SPL UNCLASSIFIED SECTION

store at 20 - 25° C (68 - 77° F). Avoid excessive heat 40° C (104° F). see end panel for batch number and expiration date TAMPER EVIDENT: DO NOT USE IF IMPRINTED SEAL IS BROKEN OR MISSING FROM BOTTLE.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

croscarmellose sodium, hypromellose, magnesium stearate, microcrystalline cellulose, povidone, pregelatinized starch, propylene glycol, sodium lauryl sulfate, stearic acid, titanium dioxide

QUESTIONS?

OTC - QUESTIONS SECTION

call 1-800-406-7984 Keep the carton. It contains important information. Contains No Aspirin. Distributed By McKesson One Post Street, San Francisco, CA 94104 www.sunmarkbrand.com

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

sunmark ® NDC 49348-921-09 See New Warnings Information arthritis pain relief Acetaminophen Extended-Release Tablets, USP 650 mg Pain Reliever/Fever Reducer For the Temporary Relief of Minor Arthritis Pain LASTS UP TO 8 HOURS Use only as directed. 50 CAPLETS * 650 mg EACH ( * capsule-shaped tablets) DO NOT USE WITH OTHER MEDICINES CONTAINING ACETAMINOPHEN COMPARE TO TYLENOL ® ARTHRITIS PAIN ACTIVE INGREDIENT † † This product is not manufactured or distributed by McNeil Consumer Healthcare, Inc. The owner of the registered trademark Tylenol ® is The Tylenol Company. sunmark ® NDC 49348-921-10 See New Warnings Information arthritis pain relief Acetaminophen Extended-Release Tablets, USP 650 mg Pain Reliever/Fever Reducer For the Temporary Relief of Minor Arthritis Pain LASTS UP TO 8 HOURS Use only as directed. 100 CAPLETS * 650 mg EACH ( * capsule-shaped tablets) THIS PACKAGE FOR HOUSEHOLDS WITHOUT YOUNG CHILDREN EASY TO OPEN BOTTLE DO NOT USE WITH OTHER MEDICINES CONTAINING ACETAMINOPHEN COMPARE TO TYLENOL ® ARTHRITIS PAIN ACTIVE INGREDIENT † † This product is not manufactured or distributed by McNeil Consumer Healthcare, Inc. The owner of the registered trademark Tylenol ® is The Tylenol Company.

Source Document

Official SPL XML cached by FDA.report · DailyMed PDF

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Legacy File Index

FolderFileDate
otcAPAP-100.jpg2012-08-20
otcAPAPArthritis.jpg2012-08-20
otcebc79b1d-d574-43e1-80f8-86bb904bdd8a.xml2012-08-20