BERKLEY JENSEN ULTRA STRENGTH 1000 mg/1
ANTACID CALCIUM CARBONATE · TABLET, CHEWABLE · BJWC
BERKLEY JENSEN ULTRA STRENGTH is a tablet, chewable containing antacid calcium carbonate at 1000 mg/1, taken oral. Manufactured by BJWC.
Key Facts
- Brand Name
- BERKLEY JENSEN ULTRA STRENGTH
- Generic Name
- ANTACID CALCIUM CARBONATE
- NDC Code (Product)
68391-033- Manufacturer
- BJWC
- Strength
- 1000 mg/1
- Dosage Form
- TABLET, CHEWABLE
- Route
- ORAL
- Marketing Status
- Application #
- M001
- Marketing Start
- 03/17/2025
Recall History
No Recall HistorySide Effects Reported to FDA
FDA FAERS database · These are reported events, not confirmed side effects
Full Prescribing Information
Indications & Usage
Uses relieves • heartburn • acid indigestion • sour stomach • upset stomach associated with these symptoms
Dosage & Administration
Directions • adults and children 12 years of age and over: chew 2-3 tablets, completely as symptoms occur, or as directed by a doctor. Do not swallow tablets whole. • do not take for symptoms that persist for more than 2 weeks unless advised by a doctor
Warnings
Warnings
Frequently Asked Questions
What is BERKLEY JENSEN ULTRA STRENGTH used for?
BERKLEY JENSEN ULTRA STRENGTH contains ANTACID CALCIUM CARBONATE. It is a tablet, chewable taken oral. Consult your doctor for specific uses.
Is BERKLEY JENSEN ULTRA STRENGTH a controlled substance?
BERKLEY JENSEN ULTRA STRENGTH is not classified as a controlled substance by the DEA.
What is the generic name for BERKLEY JENSEN ULTRA STRENGTH?
The generic name for BERKLEY JENSEN ULTRA STRENGTH is ANTACID CALCIUM CARBONATE. There are 2 other brand versions of ANTACID CALCIUM CARBONATE.
What is the NDC code for BERKLEY JENSEN ULTRA STRENGTH 1000 mg/1?
The NDC (National Drug Code) for BERKLEY JENSEN ULTRA STRENGTH 1000 mg/1 is 68391-033, listed by BJWC.