ko-lanta

Generic: aluminum hydroxide, magnesium hydroxide, dimethicone

Labeler: geri-care pharmaceuticals, corp
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name ko-lanta
Generic Name aluminum hydroxide, magnesium hydroxide, dimethicone
Labeler geri-care pharmaceuticals, corp
Dosage Form SUSPENSION
Routes
ORAL
Active Ingredients

aluminum hydroxide 200 mg/5mL, dimethicone 20 mg/5mL, magnesium hydroxide 200 mg/5mL

Manufacturer
Geri-Care Pharmaceuticals, Corp

Identifiers & Regulatory

Product NDC 57896-004
Product ID 57896-004_31a60e73-d5a3-1412-e063-6394a90a86c4
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M001
Listing Expiration 2026-12-31
Marketing Start 2020-01-01

Pharmacologic Class

Physiologic Effect
skin barrier activity [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 57896004
Hyphenated Format 57896-004

Supplemental Identifiers

RxCUI
307746
UPC
0340168220293
UNII
5QB0T2IUN0 92RU3N3Y1O NBZ3QY004S
NUI
N0000010282

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name ko-lanta (source: ndc)
Generic Name aluminum hydroxide, magnesium hydroxide, dimethicone (source: ndc)
Application Number M001 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/5mL
  • 20 mg/5mL
source: ndc
Packaging
  • 355 mL in 1 BOTTLE (57896-004-12)
source: ndc

Packages (1)

57896-004-12 355 mL in 1 BOTTLE (57896-004-12)

Ingredients (3)

aluminum hydroxide (200 mg/5mL) dimethicone (20 mg/5mL) magnesium hydroxide (200 mg/5mL)

Linked Drug Pages (1)

KO-LANTA ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "31a60e73-d5a3-1412-e063-6394a90a86c4", "openfda": {"nui": ["N0000010282"], "upc": ["0340168220293"], "unii": ["5QB0T2IUN0", "92RU3N3Y1O", "NBZ3QY004S"], "rxcui": ["307746"], "spl_set_id": ["31a6011d-5c61-d0fe-e063-6294a90ac589"], "pharm_class_pe": ["Skin Barrier Activity [PE]"], "manufacturer_name": ["Geri-Care Pharmaceuticals, Corp"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "355 mL in 1 BOTTLE (57896-004-12)", "package_ndc": "57896-004-12", "marketing_start_date": "20200201"}], "brand_name": "KO-LANTA", "product_id": "57896-004_31a60e73-d5a3-1412-e063-6394a90a86c4", "dosage_form": "SUSPENSION", "pharm_class": ["Calculi Dissolution Agent [EPC]", "Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Inhibition Small Intestine Fluid/Electrolyte Absorption [PE]", "Magnesium Ion Exchange Activity [MoA]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]", "Skin Barrier Activity [PE]", "Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]"], "product_ndc": "57896-004", "generic_name": "aluminum hydroxide, magnesium hydroxide, dimethicone", "labeler_name": "Geri-Care Pharmaceuticals, Corp", "product_type": "HUMAN OTC DRUG", "brand_name_base": "KO-LANTA", "active_ingredients": [{"name": "ALUMINUM HYDROXIDE", "strength": "200 mg/5mL"}, {"name": "DIMETHICONE", "strength": "20 mg/5mL"}, {"name": "MAGNESIUM HYDROXIDE", "strength": "200 mg/5mL"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200101", "listing_expiration_date": "20261231"}