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Generic: loratadine is used for the treatment of Deglutition Disorders Duodenal Ulcer Dyspepsia Esophagitis, Peptic Gastroesophageal Reflux Heartburn Gastrointestinal Hemorrhage Stomach Ulcer Urticaria Zollinger-Ellison Syndrome Helicobacter Infections


IMPRINT: L194     SHAPE: round
    COLOR: white

All Imprints

famotidine 20 mg - l194 round white

famotidine 20 mg oral tablet - l194 round white

maximum strength - famotidine 20 mg oral tablet - l194 round white

Boxed Warning

Boxed Warning Section

Do Not Use If Printed Foil Under Cap Is Broken Or Missing


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Otc - Purpose Section


Purpose Acid reducer

Indications & Usage Section


Use
  • relieves heartburn associated with acid indigestion and sour stomach
  • prevents heartburn associated with acid indigestion and sour stomach brought on by eating or drinking certain food and beverages

Warnings Section


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

Otc - Do Not Use Section


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.
  • if you have kidney disease, except under the advice and supervision of a doctor
  • with other acid reducers

Otc - Ask Doctor Section


Ask a doctor before use if you have
  • had heartburn over three 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

Otc - Stop Use Section


Stop use and ask a doctor if
  • your heartburn continues or worsens
  • you need to take this product for more than 14 days

Otc - Pregnancy Or Breast Feeding Section


If pregnant or breastfeeding, ask a health professional before use.

Otc - Keep Out Of Reach Of Children Section


Keep out of reach of children. In case  of overdose, get medical help or contact a Poison Control Center right away.

Dosage & Administration Section


Directions
  • adults and children 12 years and over:
    • to relieve symptoms, swallow 1 tablet with a glass of water. Do not chew.
    • to prevent symptoms, swallow 1 tablet with a glass of water at any time from 10 to 60 minutes before eating food or drinking beverages that cause heartburn
    • do not use more than 2 tablets in 24 hours
  • children under 12 years: ask a doctor

Otc - Active Ingredient Section


Active ingredient (in each tablet)

Famotidine 20 mg

Storage And Handling Section


Other information
  • store at 20°-25°C (68°-77°F)
  • protect from moisture and light

Inactive Ingredient Section


Inactive ingredients carnauba wax, colloidal silicon dioxide, croscarmellose sodium, lactose (monohydrrate), magnesium stearate, microcrystalline cellulose, polyethylene glycol, polyvinyl alcohol, talc, and titanium dioxide

Otc - Questions Section


Questions or comments? 1-800-282-3000

Boxed Warning Section


DO NOT USE IF PRINTED FOIL UNDER CAP IS BROKEN OR MISSING

General Precautions Section


Other information
  • read the directions and warnings before use
  • keep the carton, it contains important information.

Package Label.principal Display Panel




Package Label.principal Display Panel


DISCLAIMER:

"This tool does not provide medical advice, and is for informational and educational purposes only, and is not a substitute for professional medical advice, treatment or diagnosis. Call your doctor to receive medical advice. If you think you may have a medical emergency, please dial 911."

"Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service."

"This product uses publicly available data from the U.S. National Library of Medicine (NLM), National Institutes of Health, Department of Health and Human Services; NLM is not responsible for the product and does not endorse or recommend this or any other product."

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