United States · FDA National Drug Code directory
KO-LANTA
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 57896-004_31a60e73-d5a3-1412-e063-6394a90a86c4
- Product NDC
- 57896-004
- Form
- SUSPENSION
- Composition / generic term
- aluminum hydroxide, magnesium hydroxide, dimethicone
- Labeler
- Geri-Care Pharmaceuticals, Corp
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20200101
- Source listing expiry
- 20261231
Source-listed ingredients
- ALUMINUM HYDROXIDE — 200 mg/5mL
- MAGNESIUM HYDROXIDE — 200 mg/5mL
- DIMETHICONE — 20 mg/5mL
These values do not establish equivalence or a dose recommendation.
Packages
- 355 mL in 1 BOTTLE (57896-004-12) · 57896-004-12
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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