pilldic.내 손안의 약 사전
글자 크기
← 미국약 목록
미국 · 일반의약품(OTC) 설명서

EXTRA STRENGTH PAIN RELIEF PM

제형
TABLET
업체
Spirit Pharmaceutical LLC
원문 갱신
2024-12-30
가져온 날
2026-09-07
유효 성분
ACETAMINOPHEN · DIPHENHYDRAMINE HYDROCHLORIDE
DailyMed 원문·등록 이미지 확인 ↗
기타 원문Label information

Drug Facts

유효 성분유효 성분

성분·작용

Active ingredients (in each caplet) Purpose
Acetaminophen 500mg Pain reliever
Diphenhydramine HCl 25mg Nighttime Sleep aid
효능·용도Uses

for the temporary relief of occasional headaches and minor aches and pains with accompanying sleeplessness

주의사항Warnings

Liver warning

This product contains acetaminophen. Severe liver damage may occur with this product if you take

  • more than 4,000 mg of acetaminophen in 24 hours
  • with other drugs containing acetaminophen
  • 3 or more alcoholic drinks every day while you are 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 other products containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist
  • in children under 12 years of age
  • with any other products containing diphenhydramine, even one used on skin
  • if you are allergic to acetaminophen or any of the inactive ingredients in this product

Ask a doctor before use if you have

  • liver disease
  • breathing problems such as emphysema or chronic bronchitis
  • trouble urinating due to an enlargement of the prostate gland
  • glaucoma

Ask a doctor or pharmacist before use if you are

  • taking the blood thinning drug warfarin
  • taking sedatives or tranquilizers

When using this product

  • drowsiness will occur
  • avoid alcoholic drinks
  • do not drive a motor vehicle or operate machinery.

Stop use and ask a doctor if

  • sleeplessness persists continuously for more than 2 weeks. Insomnia may be a symptom of a serious underlying medical illness
  • pain gets worse or lasts for more than 10 days
  • fever gets worse or lasts more than 3 days
  • new symptoms occur
  • redness or swelling is present

These could be signs of a serious condition.

Label information

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

Label information

Keep out of reach of children.

Overdose warning

Taking more than the directed 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.

복용법·사용법Directions
  • do not take more than directed

(see Overdose warning )

adults and children 12 years of age and over:
  • take 2 caplets at bedtime or as directed by a doctor
  • do not take more than 2 caplets in a 24 hour period
children under 12 years of age:
  • 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
보관·기타 정보Other information
  • each caplet contains: magnesium 0.05 mg
  • store between 20°-25°C (68°-77°F)
  • see end panel for lot number and expiration
첨가제Inactive ingredients

FD&C blue # 1, FD&C blue # 2, hypromellose, magnesium stearate, microcrystalline cellulose, polyethylene glycol-400, povidone, pregelatinized starch, stearic acid, titanium dioxide

제조사 문의Questions or comments?

1-888-333-9792

기타 원문Label information

DISTRIBUTED BY:

SPIRIT PHARMACEUTICALS, LLC.

RONKONKOMA, NY 11779

포장 표시Principal display panel

VALUMEDS™

SEE NEW WARNINGS INFORMATION

Compare to the active ingredients in

EXTRA STRENGTH TYLENOL®PM*

EXTRA STRENGTH

PAIN RELIEF PM

PAIN RELIEVER NIGHTTIME SLEEP AID

Acetaminophen 500 mg

Diphenhydramine HCl 25 mg

[Image in the official label — see DailyMed source]

[Image in the official label — see DailyMed source]

[Image in the official label — see DailyMed source]

DailyMed Set ID: e8f71439-5c07-44ab-9c4d-42ed41eb159a · 버전 8
NDC: 68210-0099