TYLENOL® Severe Allergy Caplets

TYLENOL® Severe Allergy Caplets

Use only as directed

Description/Ingredients

Each TYLENOL® Severe Allergy Caplet contains acetaminophen 500 mg and diphenhydramine HCl 12.5 mg.

TYLENOL® Severe Allergy Caplets

Use only as directed

Actions

TYLENOL® Severe Allergy Caplets contain a clinically proven analgesic/antipyretic and antihistamine. Acetaminophen is thought to produce analgesia by elevation of the pain threshold and antipyresis through action on the hypothalamic heat regulating center. Acetaminophen is equal to aspirin in analgesic and antipyretic effectiveness and it is unlikely to produce many of the side effects associated with aspirin and aspirin-containing products. Diphenhydramine HCl is an antihistamine which helps provide temporary relief of itchy, watery eyes, runny nose, sneezing, itching of the nose or throat due to hay fever or other respiratory allergies.

TYLENOL® Severe Allergy Caplets

Use only as directed

Uses

TYLENOL® Severe Allergy Caplets:

  • temporarily relieves:
    minor aches and pains, headache, runny nose, sneezing, itching of the nose or throat and itchy, watery eyes due to hay fever
TYLENOL® Severe Allergy Caplets

Use only as directed

Dosing

TYLENOL® Severe Allergy Caplets:

Adults and children 12 years and over

  • take 2 caplets every 4 to 6 hours
  • do not take more than 8 caplets in 24 hours

Children under 12 years

  • do not use this adult product in children under 12 years of age; this will provide more than the recommended dose (overdose) and may cause liver damage
TYLENOL® Severe Allergy Caplets

Use only as directed

Warnings

TYLENOL® Severe Allergy Caplets

Alcohol warning: If you consume 3 or more alcoholic drinks every day, ask your doctor whether you should take acetaminophen or other pain relievers or fever reducers. Acetaminophen may cause liver damage.

Do not use:

  • with any other product containing acetaminophen
  • with any other product containing diphenhydramine, even one used on skin.

Ask a doctor before use if you have:

  • glaucoma
  • trouble urinating due to an enlarged prostate gland
  • a breathing problem such as emphysema or chronic bronchitis

Ask a doctor or pharmacist before use if you are taking sedatives or tranquilizers

When using this product:

  • excitability may occur, especially in children
  • marked drowsiness may occur
  • avoid alcoholic drinks
  • alcohol, sedatives and tranquilizers may increase the drowsiness effect
  • be careful when driving a motor vehicle or operating machinery

Stop use and ask a doctor if:

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

These could be signs of a serious condition.

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

Keep out of reach of children.

Overdose warning: Taking more than the recommended dose (overdose) may cause liver damage. In case of overdose, get medical help or contact a Poison Control Center right away. (1-800-222-1222). Quick medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.

Other Information:

TYLENOL® Severe Allergy Caplets:

  • store between 20-25ºC (68-77ºF)
TYLENOL® Severe Allergy Caplets

Use only as directed

PROFESSIONAL INFORMATION: OVERDOSAGE INFORMATION

Acetaminophen: Acetaminophen in massive overdosage may cause hepatic toxicity in some patients. In adults and adolescents (>/= 12 years of age), hepatic toxicity may occur following ingestion of greater than 7.5 to 10 grams over a period of 8 hours or less. Fatalities are infrequent (less than 3-4% of untreated cases) and have rarely been reported with overdoses of less than 15 grams. In children (<12 years of age), an acute overdosage of less than 150 mg/kg has not been associated with hepatic toxicity. Early symptoms following a potentially hepatotoxic overdose may include: nausea, vomiting, diaphoresis and general malaise. Clinical and laboratory evidence of hepatic toxicity may not be apparent until 48 to 72 hours postingestion. In adults and adolescents, any individual presenting with an unknown amount of acetaminophen ingested or with a questionable or unreliable history about the time of ingestion should have a plasma acetaminophen level drawn and be treated with N-acetylcysteine. For full prescribing information, refer to the N-acetylcysteine package insert. Do not await results of assays for plasma acetaminophen levels before initiating treatment with N-acetylcysteine. The following additional procedures are recommended: Promptly initiate gastric decontamination of the stomach. A plasma acetaminophen assay should be obtained as early as possible, but no sooner than four hours following ingestion. If an acetaminophen extended release product is involved, it may be appropriate to obtain an additional plasma acetaminophen level 4-6 hours following the initial acetaminophen level. If either acetaminophen level plots above the treatment line on the acetaminophen overdose nomogram, N-acetylcysteine treatment should be continued for a full course of therapy. Liver function studies should be obtained initially and repeated at 24-hour intervals. Serious toxicity or fatalities have been extremely infrequent following an acute acetaminophen overdose in young children, possibly because of differences in the way they metabolize acetaminophen. In children, the maximum potential amount ingested can be more easily estimated. If more than 150 mg/kg or an unknown amount was ingested, obtain a plasma acetaminophen level as soon as possible, but no sooner than 4 hours following ingestion. If an acetaminophen extended release product is involved, it may be appropriate to obtain an additional plasma acetaminophen level 4-6 hours following the initial acetaminophen level. If either acetaminophen level plots above the treatment line on the acetaminophen overdose nomogram, N-acetylcysteine treatment should be initiated and continued for a full course of therapy. If an assay cannot be obtained and the estimated acetaminophen ingestion exceeds 150 mg/kg, dosing with N-acetylcysteine should be initiated and continued for a full course of therapy. For additional emergency information, call your regional poison center or call the Rocky Mountain Poison Center toll-free, (1-800-525-6115).

For additional emergency information, please contact your local poison control center.
(1-800-222-1222). Alcohol Information: Chronic heavy alcohol abusers may be at increased risk of liver toxicity from excessive acetaminophen use, although reports of this event are rare. Reports usually involve cases of severe chronic alcoholics and the dosages of acetaminophen most often exceed recommended doses and often involve substantial overdose. Healthcare professionals should alert their patients who regularly consume large amounts of alcohol not to exceed recommended doses of acetaminophen.

TYLENOL® Severe Allergy Caplets

Use only as directed

How Supplied

TYLENOL® Severe Allergy:

Caplets: Yellow film-coated, imprinted with "TYLENOL® Severe Allergy" on one side - blister packs of 24.

5_8_1_cap

NOTE: These photos can be used only for identification by shape, color, and imprint. They do not depict actual or relative size.

TYLENOL® Severe Allergy Caplets

Use only as directed

Inactive Ingredients

TYLENOL® Severe Allergy Caplets: carnauba wax, cellulose, corn starch, D&C yellow #10, FD&C yellow #6 aluminum lake, hydroxypropyl cellulose, hypromellose, iron oxide, magnesium stearate, microcrystalline cellulose, polyethylene glycol, pregelatinized starch, propylene glycol, sodium citrate, sodium starch glycolate, titanium dioxide