PAIN RELIEVER PLUS- acetaminophen, caffeine tablet

Pain Reliever Plus by

Drug Labeling and Warnings

Pain Reliever Plus by is a Otc medication manufactured, distributed, or labeled by Rapid Care, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Acetaminophen 500mg

Caffeine 65mg

PURPOSE

Pain reliever/fever reducer

Pain reliever aid

Uses

temporarily relieves minor aches and pains due to:  

• headache  
• muscular aches

WARNINGS

Warnings

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.

Liver warning: This product contains acetaminophen. Severe liver damage may occur if you

take  

• more than 8 tablets 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

Caffeine warning: The recommended dose of this product contains about as much caffeine as

a cup of coffee. Limit the use of caffeine-containing medications, foods, or beverages while

taking this product because too much caffeine may cause nervousness, irritability,

sleeplessness, and, occasionally, rapid heartbeat.

In case of overdose, get medical help or contact a

Poison Control Center (1-800-222-1222) right away.

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  

• if you are allergic to acetaminophen  
• with any other drug containing
• acetaminophen (prescription or non-prescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist.

ASK DOCTOR

Ask a doctor before use if you have liver disease

ASK DOCTOR/PHARMACIST

Ask a doctor or pharmacist before use if you are taking the blood thinning drug warfarin

STOP USE

Stop use and ask a doctor if  

• any new symptoms occur  
• painful area is red or swollen
• pain gets worse or lasts for more than 10 days  
• fever gets worse or lasts for more than 3 days 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

• do not use more than directed
• adults and children 12 years and over: take 2 tablets every 6 hours; not more than 8 tablets in 24 hours
• children under 12 years: ask a doctor

Other information

store at 20-25°C (68-77° F)

INACTIVE INGREDIENT

corn starch, croscarmellose sodium, crospovidone, D&C red #27 aluminum lake, FD&C red #40 aluminum lake,

FD&C yellow #6 aluminum lake, hypromellose, microcrystalline cellulose, polyethylene glycol, povidone,pregelatinized starch, silicon dioxide, stearic acid, titanium dioxide

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PAIN RELIEVER PLUS 
acetaminophen, caffeine tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73659-014
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CAFFEINE (UNII: 3G6A5W338E) (CAFFEINE - UNII:3G6A5W338E)	CAFFEINE	65 mg
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D)	ACETAMINOPHEN	500 mg

Inactive Ingredients
Ingredient Name	Strength
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
STARCH, CORN (UNII: O8232NY3SJ)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
D&C RED NO. 27 (UNII: 2LRS185U6K)
STEARIC ACID (UNII: 4ELV7Z65AP)
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
FD&C RED NO. 40 (UNII: WZB9127XOA)
HYPROMELLOSES (UNII: 3NXW29V3WO)
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)

Product Characteristics
Color	brown	Score	score with uneven pieces
Shape	ROUND	Size	17mm
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73659-014-01	50 in 1 BOX	04/18/2022
1		2 in 1 POUCH; Type 0: Not a Combination Product
2	NDC: 73659-014-02	125 in 1 BOX	04/18/2022
2		2 in 1 POUCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part343	04/18/2022

Labeler - Rapid Care, Inc (877432778)