Pain Reliever Plus

Manufacturer
Rapid Care, Inc
Effective date
2022-04-18
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:49:15

Label at a glance#

ProductPain Reliever Plus
Active ingredientCAFFEINE, ACETAMINOPHEN
Label structure14 sections

Indications and uses

temporarily relieves minor aches and pains due to:   headache   muscular aches

Dosage and administration

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

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Acetaminophen 500mg

Caffeine 65mg

OTC - PURPOSE SECTION

Pain reliever/fever reducer

Pain reliever aid

Uses

INDICATIONS & USAGE SECTION

temporarily relieves minor aches and pains due to:  

  • headache  
  • muscular aches

WARNINGS SECTION

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.

OTC - DO NOT USE SECTION

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.

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have liver disease

OTC - ASK DOCTOR/PHARMACIST SECTION

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

OTC - STOP USE SECTION

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

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Directions

DOSAGE & ADMINISTRATION SECTION

  • 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

OTHER SAFETY INFORMATION

store at 20-25°C (68-77° F)

INACTIVE INGREDIENT SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabellabel2label2

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
307686acetaminophen 500 MG / caffeine 65 MG Oral TabletPSN1
307686acetaminophen 500 MG / caffeine 65 MG Oral TabletSCD1
307686APAP 500 MG / Caffeine 65 MG Oral TabletSY1

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
CAFFEINE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
7dea7767-9f52-b60a-5435-33cb9cc28baeProduct name420250124
6338270f-96cb-0ecb-6fbb-0a9bc78001f4Product name720250116
0ca83774-3f79-b837-5d6f-c210102f3bc8Product name620250114
41b814f3-0166-1c53-c9ef-a0794c7daf9dProduct name320221110
a590be26-846c-8659-a5a1-fb25907965dcProduct name220221110
2dc76302-91c0-4c35-ad78-99adfb049c4bProduct name120200603
e6065d4b-5ae1-476f-a40e-f2851cbb5d2bProduct name220180221
f212291f-05fe-9603-fc7e-bd73e38ce1e6Product name220161129
182f9ab4-4ab5-c449-200f-87ce2ce8e550Product name220151105
332e86c3-7875-ca6e-f934-2206d2b31996Product name120140508
56625fcc-aa34-9d30-d0e9-1c1beb37ea21Product name120140508
7dfac40f-a405-cd2e-7c06-3059ec0e1092Product name120140508
96c2be53-8e44-452d-56a2-d255b2f1af2dProduct name120140508
bf8bd5f7-495f-4022-2780-7ded7ea7ea44Product name120140508
d223c173-c39b-d764-47d4-d671d3088815Product name120140508
e01133ad-4dcd-c7f3-454b-2ff569ee160aProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73659-014-012024-01-30C16284748780-11030e365-4f48-111a-e063-dadaa90a10e2RapidCare - Pain Reliever Plus
73659-014-022024-01-30C16284748780-11030e365-4f48-111a-e063-dadaa90a10e2RapidCare - Pain Reliever Plus

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73659-014-01Pain Reliever Plus2 in 1 POUCHTABLET21
73659-014-01Pain Reliever Plus50 in 1 BOXTABLET501
73659-014-02Pain Reliever Plus125 in 1 BOXTABLET1251
73659-014-02Pain Reliever Plus2 in 1 POUCHTABLET21

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73659-014PAIN RELIEVER PLUS (ACETAMINOPHEN, CAFFEINE) TABLET [RAPID CARE, INC]1Legacy NDC, 4 package rows20220420_dcf4137a-70a1-3570-e053-2a95a90ad758.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73659-01473659-014-01, 73659-014-02

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
dcf4137a-70a2-3570-e053-2a95a90ad758dcf4137a-70a1-3570-e053-2a95a90ad7582022-04-18WarningsExact identifier
spl id: dcf4137a-70a2-3570-e053-2a95a90ad758
spl set id: dcf4137a-70a1-3570-e053-2a95a90ad758

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.