Rapidol Acetaminophen 500 Display (V)(DA)

Rapidol 500 by

Drug Labeling and Warnings

Rapidol 500 by is a Otc medication manufactured, distributed, or labeled by Pharmadel LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

RAPIDOL 500 EXTRA STRENGTH- acetaminophen tablet 
Pharmadel LLC

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Rapidol Acetaminophen 500 Display (V)(DA)

Drug Facts

Active ingredient & Purposes

.

• Active ingredient (in each tablet): Purposes
• Acetaminophen 500 mg: Pain reliever/ fever reducer

Uses

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

• a cold
• headache
• backache
• muscular aches
• toothache
• minor pain of arthritis
• premenstrual and menstrual cramps
• and to reduce fever

Warnings

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

• 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

• 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
• redness or swelling is present
• any new symptoms appear

If pregnant or breast feeding,

ask a health professional before use.

KEEP OUT OF REACH OF CHILDREN.

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

​

• ​ do not take more than directed (see LIVER WARNING)

• 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 8 tablets in 24 hours
• children under 12 years of age:
  • do not use

Other information

• store between 77-86°F (25-30°C)

Inactive ingredients

croscarmellose sodium, microcrystalline cellulose 101, povidone k30, silicon dioxide, stearic acid

Questions or comments?

+1-866-359-3478 (M-F) 9 AM to 5 PM EST or www.pharmadel.com

Dist.by/ por:

Pharmadel LLC.

New Castle, DE 19720

Prinicipal Display Panel

RAPIDOL 500  EXTRA STRENGTH
acetaminophen tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55758-439
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
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
POVIDONE K30 (UNII: U725QWY32X)
STEARIC ACID (UNII: 4ELV7Z65AP)
MICROCRYSTALLINE CELLULOSE 101 (UNII: 7T9FYH5QMK)

Product Characteristics
Color	white	Score	no score
Shape	OVAL (Capsule-Shaped Tablet)	Size	18mm
Flavor		Imprint Code	A1
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55758-439-50	25 in 1 CARTON	08/06/2024	02/01/2026
1		2 in 1 PACKET; Type 0: Not a Combination Product
2	NDC: 55758-439-01	2 in 1 PACKET; Type 0: Not a Combination Product	08/01/2024	02/01/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M013	08/01/2024	02/01/2026

Labeler - Pharmadel LLC (030129680)

Revised: 12/2025

Document Id: 4549e425-14a1-e59e-e063-6394a90ae624

34390-5

Set id: 1d9fa7ec-a509-28b2-e063-6294a90a7831

Version: 5

Effective Time: 20251206