Arthritis Pain Reliever Acetaminophen CROSPOVIDONE HYPROMELLOSE, UNSPECIFIED MAGNESIUM STEARATE MICROCRYSTALLINE CELLULOSE POVIDONE, UNSPECIFIED STARCH, CORN PROPYLENE GLYCOL SODIUM LAURYL SULFATE STEARIC ACID TITANIUM DIOXIDE ACETAMINOPHEN ACETAMINOPHEN Capsule Shaped cor116 Uses temporarily relieves minor aches and pains due to: minor pain of arthritis muscular aches backache premenstrual and menstrual cramps the common cold headache toothache temporarily reduces fever

Arthritis Pain Reliever Acetaminophen CROSPOVIDONE HYPROMELLOSE, UNSPECIFIED MAGNESIUM STEARATE MICROCRYSTALLINE CELLULOSE POVIDONE, UNSPECIFIED STARCH, CORN PROPYLENE GLYCOL SODIUM LAURYL SULFATE STEARIC ACID TITANIUM DIOXIDE ACETAMINOPHEN ACETAMINOPHEN Capsule Shaped cor116

Mfr: OTC
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Drug Facts

Composition & Profile

Active Ingredients
Drug Facts Active ingredient (in each caplet) Acetaminophen USP 650 mg
Inactive Ingredients
Inactive ingredients crospovidone hypromellose magnesium stearate microcrystalline cellulose povidone pregelatinized starch propylene glycol sodium lauryl sulfate stearic acid titanium dioxide
Strengths
650 mg
Quantities
30 tablets
Treats Conditions
Uses Temporarily Relieves Minor Aches And Pains Due To Minor Pain Of Arthritis Muscular Aches Backache Premenstrual And Menstrual Cramps The Common Cold Headache Toothache Temporarily Reduces Fever

Identifiers & Packaging

Container Type BOX
Packaging

Principal Display Panel – Carton – 650 mg NDC 68084- 777 -25 Acetaminophen Extended-release Tablets, USP Pain Reliever/Fever Reducer 650 mg 30 Tablets (5 x 6) DO NOT USE WITH OTHER MEDICINES CONTAINING ACETAMINOPHEN. Drug Facts Active Ingredient Purpose (in each caplet) Acetaminophen USP, 650 mg ................. Pain reliever/fever reducer Uses See package insert for complete Drug Facts information. 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 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. Keep out of reach of children. See package insert for additional Drug Facts warnings. Directions • do not take more than directed, see package insert for overdose warning and complete Drug Facts information. Other Information • store at 20° to 25°C (68° to 77°F). Avoid excessive heat 40°C (104°F). • FOR YOUR PROTECTION: Do not use product if blister is torn or broken. Contains No Aspirin The drug product contained in this package is from NDC # 51660-333, Ohm Laboratories Inc. Distributed by: American Health Packaging 2550 John Glenn Avenue, Suite A Columbus, OH 43217 077725 0277725/0222 650 mg Acetaminophen Extended-release Tablets Carton; Principal Display Panel – Blister – 650 mg Acetaminophen Extended-release Tablet, USP Pain Reliever/ Fever Reducer 650 mg 650 mg Acetaminophen Extended-release Tablet Blister

Package Descriptions
  • Principal Display Panel – Carton – 650 mg NDC 68084- 777 -25 Acetaminophen Extended-release Tablets, USP Pain Reliever/Fever Reducer 650 mg 30 Tablets (5 x 6) DO NOT USE WITH OTHER MEDICINES CONTAINING ACETAMINOPHEN. Drug Facts Active Ingredient Purpose (in each caplet) Acetaminophen USP, 650 mg ................. Pain reliever/fever reducer Uses See package insert for complete Drug Facts information. 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 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. Keep out of reach of children. See package insert for additional Drug Facts warnings. Directions • do not take more than directed, see package insert for overdose warning and complete Drug Facts information. Other Information • store at 20° to 25°C (68° to 77°F). Avoid excessive heat 40°C (104°F). • FOR YOUR PROTECTION: Do not use product if blister is torn or broken. Contains No Aspirin The drug product contained in this package is from NDC # 51660-333, Ohm Laboratories Inc. Distributed by: American Health Packaging 2550 John Glenn Avenue, Suite A Columbus, OH 43217 077725 0277725/0222 650 mg Acetaminophen Extended-release Tablets Carton
  • Principal Display Panel – Blister – 650 mg Acetaminophen Extended-release Tablet, USP Pain Reliever/ Fever Reducer 650 mg 650 mg Acetaminophen Extended-release Tablet Blister

Overview

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

Indications & Usage

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

Dosage & Administration

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

Warnings & Precautions
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 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 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. Ask a doctor before use if you have liver disease. Ask a doctor or pharmacist before use if you are taking the blood thinning drug warfarin. Stop use and ask a doctor if 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. If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. Overdose warning: 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.
Purpose

Purpose Pain reliever/fever reducer

Do Not Use

Do not use 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.

Stop Use & Ask a Doctor

Stop use and ask a doctor if 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.

Keep Out of Reach of Children

Keep out of reach of children. Overdose warning: 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.

Questions

Questions? about the drug product, call Sun Pharmaceutical Industries, Inc. at 1-800-406-7984 about the packaging, call American Health Packaging at 1-800-707-4621 Contains No Aspirin PACKAGING INFORMATION American Health Packaging unit dose blisters contain drug product from Ohm Laboratories Inc. as follows: (650 mg / 30 UD) NDC 68084-777-25 packaged from NDC 51660-333 Distributed by: American Health Packaging Columbus, OH 43217 8277725/0121


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