ALLPANTO S description, usages, side effects, indications, overdosage, supplying and lots more!

ALLPANTO S

SAMSUNG PHARM IND. CO., LTD.
SAMSUNG PHARM IND. CO., LTD.

  • Description
  • Clinical Pharmacology
  • Indications & Usage
  • Contraindications
  • Warnings
  • Precautions
  • Side Effects
  • Overdosage
  • Dosage & Administration
  • How Supplied
  • Patient Counseling Information
  • Supplemental Patient Material
  • Boxed Warning
  • Patient Package Insert
Drug Facts



FULL PRESCRIBING INFORMATION

Active ingredient

Active ingredients:
Acetaminophen   162.5mg     
Pseudoephedrine HCl   15mg
Dextromethorphan hydrobromide   7.5mg
Chlorpheniramine Maleate   1mg

Inactive ingredients:
lactose, corn starch, Hydroxypropylcellulose, calcium carboxymethylcellulose, colloidal anhydrous silica, magnesium stearate, hydroxypropyl methylcellulose, propylene glycol, titanium oxide, sucralose

Purpose

Uses:
The relief of common cold symptoms (nasal mucus, nasal obstruction, sneeze, throat pain, cough, chill, fever, headache, arthralgia, myalgia)

Direction:
Adults and children 15 years and over: take 2 tables, 3 times a day

Warnings:
Ask a doctor or pharmacist before use if you are regularly drinking over three cups of alcohol per day or taking any other antipyretic and analgesics. Liver can be damaged if taken.

Caution if taken
  1) Keep direction
  2) Not taken with anti-tussive, expectorant, antipyretic, antihistamine, sedative
  3) Let children take drug by protector
  4) In infants younger than 3 months to avoid taking more than three months also infant under 2 years of age to be a doctor, and if it is not needed is not to take your medicine
      Administered to infants younger than 2 years if the drug should be carefully monitored for parents to know

Caution if taken
  1) While taking a rash, redness, nausea, vomiting, constipation, anorexia, dysuria, dizziness and other symptoms when you stop asking your doctor or pharmacist
  2) Stop taking medicine and ask a doctor or pharmacist before use even though adverse events are rarely reported below.
    - Rash, edema, breast burden, pale complexion, cold hand and foot, cold sweat, shortness of breath
    - High fever, rash, flare, bubble on whole skin, mouth, eye mucosa
    - Asthma
  3) Barbital induced drug, tri-cyclic antidepressant and alcohol can reduce ability of acetaminophen metabolism and increase plasma half life. Alcohol could increase liver toxicity of acetaminophen overdose
  4) If you get drowsy, Be careful when driving a motor vehicle or operating machinery
  5) Please don’t take drug and ask doctor or pharmacist if you can not feel better by several dose.
  6) Don’t take for a long term

Contraindication:
1) If you are anaphylactic to this drug (e.g., rash, flare, pruritis, edema)
2) Asthma patient after taking this drug or other anti-cold, antipyretic and analgesic

Ask a doctor or pharmacist before use
 1) Family history to urticaria, contact dermatitis, bronchial asthma, allergic rhinitis, migrane, food allergy
 2) Allergy experience to this drug (fever, rash, arthritis, asthma, pruritis)
 3) Child below 14 years may be Infected by Chickenpox or influenza
 4) Disease of Liver, kidney and thyroid disease, Diabetes, hypertension, weakling, high-fever
 5) Glaucoma, dysuria
 6) Pregnant or breast-feeding
 7) People treated by MD or dentist

Caution of storage:
 1) Keep out of reach of children
 2) Avoid sunlight and keep in cool and low humid place
 3) Don't abuse and replace with other container

Keep out of reach of children:
Keep out of reach of children

Other information:
Store in a hermetic and light protected container. Store between 1C to 30C. 36 months from the manufacturing date

Uses

indication and usage:
Adults and children 15 years and over: take 2 tables, 3 times a day

ALLPANTO S

ACETAMINOPHEN, PSEUDOEPHEDRINE HYDROCHLORIDE, DEXTROMETHORPHAN HYDROBROMIDE, CHLORPHENIRAMINE MALEATE TABLET

Product Information

Product Type Human otc drug label Item Code (Source) NDC:49789-010
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
ACETAMINOPHEN ACETAMINOPHEN 162.5 mg
Pseudoephedrine Hydrochloride Pseudoephedrine 15 mg
DEXTROMETHORPHAN HYDROBROMIDE DEXTROMETHORPHAN 7.5 mg
Chlorpheniramine Maleate CHLORPHENIRAMINE 1 mg

Inactive Ingredients

Ingredient Name Strength
LACTOSE
STARCH, CORN
hydroxypropyl cellulose
MAGNESIUM STEARATE
propylene glycol
titanium dioxide
Sucralose

Product Characteristics

Color Size Imprint Code Shape
white 17 mm SSAS OVAL

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:49789-010-01 488 in 1 BLISTER PACK

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part343 2012-03-01


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Be sure to consult your doctor before taking any medication!
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