Active Ingredient
Calcium carbonate 1000 mg
The following Structured Product Label (SPL) was submitted to the FDA by Anhui Jiuhe Health Industry Co., Ltd for the product Antacid- Calcium Carbonate (NDC 87745-001). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient, purpose, use, warnings, do not use, when using, stop use, ask doctor, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Calcium carbonate 1000 mg
Antacid
Relieves heartburn, acid indigestion, sour stomach, upset stomach associated with these symptoms
Ask a doctor or pharmacist before use if you are presently taking a prescription drug. Antacids may interact with certain prescription drugs.
Do not take more than 8 tablets in 24 hours. Do not use the maximum dosage for more than 2 weeks except under advice and supervision of a doctor. If pregnant, do not take more than 4 tablets in 24 hours.
Do not swallow tablets whole. Keep the container tightly closed.
Do not take for symptoms that persist for more than 2 weeks unless advised by a doctor.
If pregnant or breast-feeding, ask a health professional before use.
Keep out of reach of children.
Adults and children 12 years of age and over: chew 2–4 tablets completely as symptoms occur, 2 times daily or as directed by a doctor.
Each tablet contains calcium 400 mg. Store at room temperature 68–77°F (20–25°C). Contains FD&C Yellow No.5 (tartrazine) as color additive.
Corn starch, FD&C Blue No.1 aluminum lake, FD&C Yellow No.5 aluminum lake, flavors, magnesium stearate, maltitol, sucralose, sucrose
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