melox

Generic: aluminum hydroxide, magnesium hydroxide, simethicone

Labeler: belmora llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name melox
Generic Name aluminum hydroxide, magnesium hydroxide, simethicone
Labeler belmora llc
Dosage Form SUSPENSION
Routes
ORAL
Active Ingredients

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

Manufacturer
Belmora LLC

Identifiers & Regulatory

Product NDC 27854-115
Product ID 27854-115_54fbe2ae-c375-4a87-bee6-d1abf60360c0
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M001
Listing Expiration 2026-12-31
Marketing Start 2018-06-01

Pharmacologic Class

Classes
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]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 27854115
Hyphenated Format 27854-115

Supplemental Identifiers

RxCUI
307746
UPC
0853030002311
UNII
5QB0T2IUN0 92RU3N3Y1O NBZ3QY004S

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 melox (source: ndc)
Generic Name aluminum hydroxide, magnesium hydroxide, simethicone (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 (27854-115-01)
source: ndc

Packages (1)

27854-115-01 355 mL in 1 BOTTLE (27854-115-01)

Ingredients (3)

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

Linked Drug Pages (1)

Melox ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "54fbe2ae-c375-4a87-bee6-d1abf60360c0", "openfda": {"upc": ["0853030002311"], "unii": ["5QB0T2IUN0", "92RU3N3Y1O", "NBZ3QY004S"], "rxcui": ["307746"], "spl_set_id": ["d41f0b26-5add-4045-9754-37d70d120d28"], "manufacturer_name": ["Belmora LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "355 mL in 1 BOTTLE (27854-115-01)", "package_ndc": "27854-115-01", "marketing_start_date": "20180601"}], "brand_name": "Melox", "product_id": "27854-115_54fbe2ae-c375-4a87-bee6-d1abf60360c0", "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": "27854-115", "generic_name": "Aluminum hydroxide, Magnesium hydroxide, Simethicone", "labeler_name": "Belmora LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Melox", "active_ingredients": [{"name": "ALUMINUM HYDROXIDE", "strength": "200 mg/5mL"}, {"name": "DIMETHICONE, UNSPECIFIED", "strength": "20 mg/5mL"}, {"name": "MAGNESIUM HYDROXIDE", "strength": "200 mg/5mL"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20180601", "listing_expiration_date": "20261231"}