Rapidol

Manufacturer
Pharmadel LLC
Effective date
2026-03-20
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:51:00

Label at a glance#

ProductRapidol
Active ingredientACETAMINOPHEN
Label structure9 sections

Indications and uses

For the temporary relief of minor aches and pains due to: the common cold headache backache muscular aches toothache minor pain of arthritis premenstrual and menstrual cramps temporarily reduces fever

Dosage and administration

Age Dose adults and children 12 years of age and older take 2 tablets every 6 hours while symptoms last. do not take more than 6 tablets in 24 hours, unless directed by a doctor children under 12 years of age consult a doctor

Label contents#

Full prescribing information#

Drug Facts

SPL UNCLASSIFIED SECTION

.

Active ingredient & Purposes

OTC - ACTIVE INGREDIENT SECTION

OTC - PURPOSE SECTION

Active ingredient (in each tablet)Purposes
Acetaminophen 500 mgPain reliever/ fever reducer

Uses

INDICATIONS & USAGE SECTION

For the temporary relief of minor aches and pains due to:

  • the common cold
  • headache
  • backache
  • muscular aches
  • toothache
  • minor pain of arthritis
  • premenstrual and menstrual cramps
  • temporarily reduces fever

Warnings

WARNINGS SECTION

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

  • more than 6 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

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

OTC - DO NOT USE SECTION

  • 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 allergic to of the inactive ingredients in this product

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

liver disease

Ask a doctor or pharmacist before use if you are

OTC - ASK DOCTOR/PHARMACIST SECTION

taking the blood thinning drug warfarin

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • pain gets worse or lasts more than 10 days
  • fever gets worse or lasts more than 3 days
  • redness or swelling is present
  • any new symptoms occur

These could be signs of a serious condition.

If pregnant or breast feeding,

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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 for children even if you do not notice any signs or symptoms.

Directions

DOSAGE & ADMINISTRATION SECTION

AgeDose
adults and children 12 years of age and older
  • take 2 tablets every 6 hours while symptoms last.
  • do not take more than 6 tablets in 24 hours, unless directed by a doctor
children under 12 years of age
  • consult a doctor

Other information

OTHER SAFETY INFORMATION

  • store between 77-86°F (25-30°C)

Inactive ingredients

INACTIVE INGREDIENT SECTION

corn starch, hypromellose, magnesium stearate, microcrystalline cellulose, polyethylene glycol, povidone, stearic acid, talc, titanium dioxide

Dist. by/ por:

SPL UNCLASSIFIED SECTION

PHARMADEL LLC

New Castle, DE 19720

+1-866-359-3478

Prinicipal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

RAPIDOL PDPRAPIDOL PDP

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
198439acetaminophen 500 MG Oral CapsulePSN3
198439acetaminophen 500 MG Oral CapsuleSCD3
198439APAP 500 MG Oral CapsuleSY3

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
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DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55758-503-24Rapidol1 in 1 CARTONCAPSULE, COATED13
55758-503-24Rapidol24 in 1 BOTTLECAPSULE, COATED243

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
55758-50355758-503-24

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 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
RapidolACETAMINOPHENPharmadel LLC3a210860-1fc1-e496-e063-6394a90a87052026-03-20WarningsExact identifier
ndc (package): 55758-503-24
ndc (product): 55758-503
ndc11 (package): 55758050324
spl id: 4d7ad07e-3403-c0cf-e063-6294a90a0c93
spl set id: 3a210860-1fc1-e496-e063-6394a90a8705

Reported adverse events (FAERS/openFDA)#

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