Wal-Mart Arthritis Pain Drug Facts

Drug Details [pdf]

EQUATE ARTHRITIS PAIN- acetaminophen tablet, film coated, extended release
Wal-Mart Stores Inc

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Wal-Mart Arthritis Pain Drug Facts

Active ingredient (in each caplet)

Acetaminophen 650 mg

Purpose

Pain reliever/fever reducer

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

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.

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 information

store at 20-25°C (68-77°F). Avoid excessive heat 40°C (104°F).

Inactive ingredients

carnauba wax, colloidal silicon dioxide, croscarmellose sodium, hypromellose, magnesium stearate, maltodextrin, microcrystalline cellulose, polyethylene glycol, polysorbate 80, povidone, pregelatinized starch, stearic acid, titanium dioxide

Questions or comments?

1-888-287-1915

Principal Display Panel

SEE NEW WARNING

Compare to Tylenol® 8HR Arthritis Pain active ingredient

Arthritis Pain

Acetaminophen Extended-Release Tablets, 650 mg

Pain Reliever / Fever Reducer

For the Temporary Relief of Minor Arthritis Pain

24 CAPLETS†

650 mg EACH

†Capsule-Shaped Tablets

Actual Size

EQUATE ARTHRITIS PAIN
acetaminophen tablet, film coated, extended release

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 49035-544
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D)	ACETAMINOPHEN	650 mg

Ingredient Name	Strength
Inactive Ingredients
CARNAUBA WAX (UNII: R12CBM0EIZ)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
HYPROMELLOSES (UNII: 3NXW29V3WO)
MAGNESIUM STEARATE (UNII: 70097M6I30)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
POVIDONE (UNII: FZ989GH94E)
STEARIC ACID (UNII: 4ELV7Z65AP)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)

Product Characteristics
Color	WHITE	Score	no score
Shape	CAPSULE (caplet)	Size	19mm
Flavor		Imprint Code	L544
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC: 49035-544-62	1 in 1 CARTON	05/16/2000	06/07/2018
1		24 in 1 BOTTLE; Type 0: Not a Combination Product
2	NDC: 49035-544-78	1 in 1 CARTON	06/08/2005	06/25/2018
2		100 in 1 BOTTLE; Type 0: Not a Combination Product
3	NDC: 49035-544-83	225 in 1 BOTTLE; Type 0: Not a Combination Product	11/23/2010	03/23/2015
4	NDC: 49035-544-87	2 in 1 PACKAGE	03/03/2012	03/07/2016
4	NDC: 49035-544-47	150 in 1 BOTTLE; Type 0: Not a Combination Product
5	NDC: 49035-544-01	325 in 1 BOTTLE; Type 0: Not a Combination Product	08/13/2014	06/25/2018

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
ANDA	ANDA075077	05/16/2000	06/25/2018

Labeler - Wal-Mart Stores Inc (051957769)

Revised: 6/2019

Document Id: 253dc756-0415-4c72-be59-fc7aecfc0fc7

Set id: baac3c00-a651-4fd8-92f8-d790f1d0b1b7

Version: 7

Effective Time: 20190613

Wal-Mart Stores Inc