acid controller complete description, usages, side effects, indications, overdosage, supplying and lots more!

acid controller complete

Safeway

  • 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
Safeway Inc. Acid Controller Complete Drug Facts

FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredient (in each chewable tablet)

Famotidine 10 mg

Calcium carbonate 800 mg

Magnesium hydroxide 165 mg

Purpose

Acid reducer

Antacid

Uses

relieves heartburn associated with acid indigestion and sour stomach

Warnings

Allergy alert: Do not use if you are allergic to famotidine or other acid reducers

Do not use

  • if you have trouble or pain swallowing food, vomiting with blood, or bloody or black stools. These may be signs of a serious condition. See your doctor.
  • with other acid reducers

Ask a doctor before use if you have

  • had heartburn over 3 months. This may be a sign of a more serious condition.
  • heartburn with lightheadedness, sweating, or dizziness
  • chest pain or shoulder pain with shortness of breath; sweating; pain spreading to arms, neck or shoulders; or lightheadedness
  • frequent chest pain
  • frequent wheezing, particularly with heartburn
  • unexplained weight loss
  • nausea or vomiting
  • stomach pain

Ask a doctor or pharmacist before use if you are

presently taking a prescription drug. Antacids may interact with certain prescription drugs.

Stop use and ask a doctor if

  • your heartburn continues or worsens
  • you need to take this product for more than 14 days

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. (1-800-222-1222)

Directions

  • adults and children 12 years and over:
  • do not swallow tablet whole: chew completely
  • to relieve symptoms, chew 1 tablet before swallowing
  • do not use more than 2 chewable tablets in 24 hours
  • children under 12 years: ask a doctor

Other information

  • each tablet contains: calcium 320 mg; magnesium 70 mg
  • Phenylketonurics: Contains phenylalanine 2.2 mg per tablet 
  • read the directions and warnings before use
  • read the bottle label. It contains important information.
  • store at 20-25°C (68-77°F)
  • protect from moisture

Inactive ingredients

anhydrous lactose, artificial berry flavor, aspartame, D&C red no. 7 calcium lake, dextrates, FD&C blue no. 1 aluminum lake, FD&C red no. 40 aluminum lake, glyceryl monostearate, lactose monohydrate, magnesium stearate, microcrystalline cellulose, polyacrylate dispersion, polysorbate 80, povidone, pregelatinized starch, sodium starch glycolate, talc

1-888-SAFEWAY

Principal Display Panel

Compare to Pepcid Complete® active ingredients

Dual Action

Acid Controller Complete

Famotidine 10 mg - Calcium Carbonate 800 mg - Magnesium Hydroxide 165 mg Tablets (Chewable)

Acid Reducer plus Antacid

Just One Tablet Relieves Heartburn Due to Acid Indigestion

ACTUAL SIZE

Berry Flavor

Principal Display Panel
Acid Controller Complete Label Image 1 Acid Controller Complete Label Image 2

acid controller complete

famotidine, calcium carbonate and magnesium hydroxide TABLET, CHEWABLE

Product Information

Product Type Human otc drug label Item Code (Source) NDC:21130-321
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
FAMOTIDINE FAMOTIDINE 10 mg
magnesium hydroxide MAGNESIUM CATION 165 mg
CALCIUM CARBONATE 800 mg

Inactive Ingredients

Ingredient Name Strength
ASPARTAME
DEXTRATES
GLYCERYL MONOSTEARATE
cellulose, microcrystalline
ANHYDROUS LACTOSE
lactose monohydrate
MAGNESIUM STEARATE
polysorbate 80
povidone
talc

Product Characteristics

Color Size Imprint Code Shape
PINK (mottled) 17 mm L321 ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:21130-321-63 25 in 1 BOTTLE
2 NDC:21130-321-71 50 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA077355 2008-08-06


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Be sure to consult your doctor before taking any medication!
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