Pain Relief Extra Strength
Acetaminophen · Capsule, Liquid Filled · Oral
Active ingredient
Active ingredient (in each capsule) Acetaminophen 500 mg
Purpose
Purpose Pain reliever/ fever reducer
Uses
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
Warnings
Warnings Warnings Liver warning: This product contains acetaminophen. The maximum daily dose of this product is 6 softgels (3,000 mg) in 24 hours. 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 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 have ever had an allergic reaction to this product or any of its ingredients Ask a doctor before use if the user has 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.
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 have ever had an allergic reaction to this product or any of its ingredients
Ask a doctor before use
Ask a doctor before use if the user has liver disease.
Ask a doctor or pharmacist
Ask a doctor or pharmacist before use if you are taking the blood thinning drug warfarin.
Stop use and 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.
Pregnancy or breast-feeding
If pregnant or breast-feeding, ask a health professional before use.
Keep out of reach of children
Keep out of reach of children.
Directions
Directions Do not take more than directed (see Overdose warning ) Adults and children 12 years of age and over take 2 softgels every 4 to 6 hours while symptoms last do not take more than 6 softgels in 24 hours unless directed by a doctor do not take more than 10 days unless diredted by doctor Children 12 years of age ask a doctor
Other information
Other information store at room temperature 15°-30°C (59°-86°F)
Inactive ingredients
Inactive ingredients FD&C red #40, FD&C yellow #6, gelatin, glycerin, polyethylene glycol, povidone, propylene glycol, purified water, sorbitol special and white edible ink Manufactured by: Humanwell PuraCap Pharmaceutical (Wuhan) Ltd. Wuhan, Hubei 430206, China
Label text from the FDA structured product label by Humanwell PuraCap Pharmaceutical (Wuhan), Ltd. (revised Nov 25, 2024). Long sections are shortened; the complete label is on DailyMed.
Active ingredients
- Acetaminophen in 1 product
Pain Relief Extra Strength NDC products (1)
| NDC | Strength & form | Labeler | Type |
|---|---|---|---|
| 53345-019 | Acetaminophen 500 mg/1 Capsule, Liquid Filled | Humanwell PuraCap Pharmaceutical (Wuhan), Ltd. | OTC MONOGRAPH DRUG |
Frequently asked questions
What is Pain Relief Extra Strength used for?
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
Who makes Pain Relief Extra Strength?
Pain Relief Extra Strength is listed by 1 labeler in the FDA NDC directory, including Humanwell PuraCap Pharmaceutical (Wuhan), Ltd..