FDA.reportPublic FDA data

Rapidol Acetaminophen 500 (V)

Manufacturer
Pharmadel LLC
Effective date
2026-07-16
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
daily-update
Hydrated at
2026-09-01 13:01:55

Label at a glance#

ProductRapidol 500 Extra Strength
Active ingredientACETAMINOPHEN
Label structure8 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 from arthritis premenstrual and menstrual cramps temporarily reduces fever

Dosage and administration

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#

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 from 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 8 tablets in 24 hours, which is the maximum daily amount for this product
  • 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 non-prescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist.
  • if allergic to any of the 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 appear. These could be signs of a serious condition.

If pregnant or breastfeeding,

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

  • 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

colloidal silicon dioxide, corn starch, microcrystalline cellulose, povidone, sodium starch glycolate, stearic acid

Dist.by/ por:

SPL UNCLASSIFIED SECTION

Pharmadel LLC.

New Castle, DE 19720

+1-866-359-3478 or

www.pharmadel.com

Do not use if seal under cap is broken, torn or missing.

Prinicipal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Rapidol Acetaminofen 500Rapidol Acetaminofen 500.

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
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Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
55758-43955758-439-50, 55758-439-01, 55758-439-24

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
ACETAMINOPHEN362O9ITL9DACTIB
SILICON DIOXIDEETJ7Z6XBU4IACT
POVIDONE K30U725QWY32XIACT
STEARIC ACID4ELV7Z65APIACT
MICROCRYSTALLINE CELLULOSE 112X7XJ6RM9Q2IACT
STARCH, CORNO8232NY3SJIACT
SODIUM STARCH GLYCOLATE TYPE AH8AV0SQX4DIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
62026-03-13full-release2026-06-01 01:50:22
52025-12-06monthly-update2026-06-03 17:45:26

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
Rapidol 500 Extra StrengthACETAMINOPHENPharmadel LLC1d9fa7ec-a509-28b2-e063-6294a90a78312026-07-16WarningsExact identifier
ndc (package): 55758-439-01
ndc (package): 55758-439-50
ndc (package): 55758-439-24
ndc (product): 55758-439
ndc11 (package): 55758043950
ndc11 (package): 55758043924
ndc11 (package): 55758043901
spl id: 56bfcbc6-794c-6074-e063-6394a90a6215
spl set id: 1d9fa7ec-a509-28b2-e063-6294a90a7831

Reported adverse events (FAERS/openFDA)#

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