RIGHT REMEDIES PAIN RELIEF CAPLET- acetaminophen tablet, coated

RIGHT REMEDIES Pain Relief Caplet by

Drug Labeling and Warnings

RIGHT REMEDIES Pain Relief Caplet by is a Otc medication manufactured, distributed, or labeled by Strive Pharmaceuticals Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient (in each caplet)

Acetaminophen 500mg

Purpose

Pain reliever/fever reducer

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

Liver warning: This product contains acetaminophen.
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

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 have ever had an allergic reaction to this product or any of its ingredients.

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. Prompt medical attention is critical for adults as well as children even if you do not notice any signs or symptoms.

Directions

Do not take more than directed. SEE OVERDOSE WARNING.

• adults & children12 years of ageand over:

  take 2 caplets every 6 hours while symptoms last

  do not take more than 6 caplets in 24 hours, unless directed by doctor

  do not take more than 10 days, unless directed by a doctor

• children under12 years of age: ask a doctor

Other information

store at room temperature between 20 - 25ºC (68-77ºF).
avoid excessive heat, cold and humidity.
close cap tightly after use.
TAMPER EVIDENT: Do not use if imprinted safety seal is broken or missing.

Inactive ingredients

hydroxypropyl methylcellulose, maltodextrin, microcrystalline cellulose, polyethylene glycol, povidone, sodium starch glycolate, starch, stearic acid

Questions or comments?

Call 1 (888) 577 - 8033

SPL UNCLASSIFIED SECTION

†compare to active ingredient in TYLENOL® Extra Strength Caplets

EXTRA STRENGTH

Distributed by: STRIVE PHARMACEUTICALS INC.
East Brunswick, NJ 08816

READ AND KEEP OUTER PACKAGE FOR COMPLETE PRODUCT INFORMATION

†This product is not manufactured or distributed by Johnson & Johnson Consumer Inc., McNeil Consumer Healthcare Division., owner of the registered trademark Tylenol® Extra Strength Caplets.

Packaging

INGREDIENTS AND APPEARANCE

RIGHT REMEDIES PAIN RELIEF CAPLET 
acetaminophen tablet, coated

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70692-141
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D)	ACETAMINOPHEN	500 mg

Inactive Ingredients
Ingredient Name	Strength
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)
SODIUM STARCH GLYCOLATE TYPE A (UNII: H8AV0SQX4D)
STARCH, CORN (UNII: O8232NY3SJ)
STEARIC ACID (UNII: 4ELV7Z65AP)

Product Characteristics
Color	white	Score	no score
Shape	capsule	Size	18mm
Flavor		Imprint Code	S500
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70692-141-42	24 in 1 PACKAGE; Type 0: Not a Combination Product	04/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part343	04/01/2020

Labeler - Strive Pharmaceuticals Inc. (080028013)