- SPL UNCLASSIFIED SECTION
- Active ingredient (in each tablet)
- Purpose
- Uses
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Warnings
Allergy alert: Do not use if you are allergic to cimetidine 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
- frequent chest pain
- frequent wheezing, particularly with heartburn
- unexplained weight loss
- nausea or vomiting
- stomach pain
- 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
- kidney disease
- liver disease
Ask a doctor or pharmacist before use if
you are taking a prescription drug. Acid reducers may interact with certain prescription drugs.
- 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.
-
Directions
- adults and children 12 years and older:
▪ to relieve symptoms, swallow 1 tablet with a glass of water
▪ to prevent symptoms, swallow 1 tablet with a glass of water right before or any time up to 30 minutes before eating food or drinking beverages that cause heartburn
▪ do not take more than 2 tablets in 24 hours - children under 12 years: ask a doctor
- adults and children 12 years and older:
- Other information
- Inactive ingredients
- Questions?
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
TAGAMET
cimetidine tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63029-222 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CIMETIDINE (UNII: 80061L1WGD) (CIMETIDINE - UNII:80061L1WGD) CIMETIDINE 200 mg Inactive Ingredients Ingredient Name Strength POWDERED CELLULOSE (UNII: SMD1X3XO9M) STARCH, CORN (UNII: O8232NY3SJ) HYPROMELLOSES (UNII: 3NXW29V3WO) MAGNESIUM STEARATE (UNII: 70097M6I30) POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) POLYSORBATE 80 (UNII: 6OZP39ZG8H) POVIDONE (UNII: FZ989GH94E) SODIUM LAURYL SULFATE (UNII: 368GB5141J) SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) Product Characteristics Color white Score no score Shape DIAMOND Size 13mm Flavor Imprint Code TAGAMET;200 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63029-222-02 1 in 1 BOX 06/01/2012 1 6 in 1 BLISTER PACK; Type 0: Not a Combination Product 2 NDC:63029-222-01 1 in 1 BOX 06/01/2012 2 30 in 1 BLISTER PACK; Type 0: Not a Combination Product 3 NDC:63029-222-03 1 in 1 BOX 06/01/2012 3 50 in 1 BLISTER PACK; Type 0: Not a Combination Product 4 NDC:63029-222-04 4 in 1 BOX 06/01/2019 4 10 in 1 BLISTER PACK; Type 0: Not a Combination Product 5 NDC:63029-222-05 4 in 1 BOX 06/01/2019 5 9 in 1 BLISTER PACK; Type 0: Not a Combination Product 6 NDC:63029-222-06 7 in 1 BOX 06/01/2012 6 10 in 1 BLISTER PACK; Type 0: Not a Combination Product 7 NDC:63029-222-70 1 in 1 CARTON 06/01/2012 7 70 in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date NDA NDA020238 06/01/2012 Labeler - Medtech Products Inc. (122715688)