ARTHRITIS PAIN RELIEF TEMPORARY MINOR- acetaminophen tablet, film coated, extended release
Kroger Company

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Kroger Co. Arthritis Pain Relief 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?

1-800-632-6900

Principal Display Panel

BONUS! + 20 Free

COMPARE TO the active ingredient of TYLENOL® 8HR ARTHRITIS PAIN

See end panel

SEE NEW WARNING

Temporary, Minor

Arthritis Pain Relief

Acetaminophen

Extended-Release Tablets, 650 mg

Pain Reliever/Fever Reducer

EXTENDED RELEASE

actual size

120

100 CAPLETS*

650 mg EACH

(*capsule-shaped tablets)

ARTHRITIS PAIN RELIEF TEMPORARY MINOR
acetaminophen tablet, film coated, extended release

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:30142-544
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)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
MAGNESIUM STEARATE (UNII: 70097M6I30)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)
STEARIC ACID (UNII: 4ELV7Z65AP)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)

Product Characteristics
Color	WHITE	Score	no score
Shape	OVAL	Size	19mm
Flavor		Imprint Code	L544
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:30142-544-78	1 in 1 CARTON	06/06/2000	08/31/2021
1		100 in 1 BOTTLE; Type 0: Not a Combination Product
2	NDC:30142-544-71	1 in 1 CARTON	06/13/2000	09/26/2016
2		50 in 1 BOTTLE; Type 0: Not a Combination Product
3	NDC:30142-544-85	250 in 1 BOTTLE; Type 0: Not a Combination Product	04/21/2013	09/11/2015
4	NDC:30142-544-47	1 in 1 CARTON	03/15/2014	02/29/2020
4		150 in 1 BOTTLE; Type 0: Not a Combination Product
5	NDC:30142-544-76	1 in 1 CARTON	08/09/2016	08/09/2016
5		120 in 1 BOTTLE; Type 0: Not a Combination Product
6	NDC:30142-544-62	1 in 1 CARTON	06/01/2018	08/31/2021
6		24 in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
ANDA	ANDA075077	06/06/2000	08/31/2021

Labeler - Kroger Company (006999528)

Revised: 10/2021

Document Id: 42a3b327-4d49-4253-9cf9-f49dda73713a

Set id: 86208a98-36a8-4d0b-ba4e-b974ad478067

Version: 9

Effective Time: 20211019

Kroger Company