mylanta maximum strength vanilla caramel flavor

Generic: antacid and anti gas aluminum hydroxide magnesium hydroxide and simethicone

Labeler: infirst healthcare inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name mylanta maximum strength vanilla caramel flavor
Generic Name antacid and anti gas aluminum hydroxide magnesium hydroxide and simethicone
Labeler infirst healthcare inc.
Dosage Form SUSPENSION
Routes
ORAL
Active Ingredients

aluminum hydroxide 800 mg/10mL, dimethicone 80 mg/10mL, magnesium hydroxide 800 mg/10mL

Manufacturer
Infirst Healthcare Inc.

Identifiers & Regulatory

Product NDC 62372-504
Product ID 62372-504_0bb0df3b-05ce-5c5b-e063-6394a90ab91a
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M001
Listing Expiration 2026-12-31
Marketing Start 2016-03-21

Pharmacologic Class

Physiologic Effect
skin barrier activity [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 62372504
Hyphenated Format 62372-504

Supplemental Identifiers

RxCUI
237870
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 mylanta maximum strength vanilla caramel flavor (source: ndc)
Generic Name antacid and anti gas aluminum hydroxide magnesium hydroxide and simethicone (source: ndc)
Application Number M001 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 800 mg/10mL
  • 80 mg/10mL
source: ndc
Packaging
  • 355 mL in 1 BOTTLE, PLASTIC (62372-504-12)
source: ndc

Packages (1)

62372-504-12 355 mL in 1 BOTTLE, PLASTIC (62372-504-12)

Ingredients (3)

aluminum hydroxide (800 mg/10mL) dimethicone (80 mg/10mL) magnesium hydroxide (800 mg/10mL)

Linked Drug Pages (1)

Mylanta Maximum Strength Vanilla Caramel Flavor ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0bb0df3b-05ce-5c5b-e063-6394a90ab91a", "openfda": {"nui": ["N0000010282"], "unii": ["5QB0T2IUN0", "92RU3N3Y1O", "NBZ3QY004S"], "rxcui": ["237870"], "spl_set_id": ["ace5cae4-3a78-41c3-987d-59ce22dca2ac"], "pharm_class_pe": ["Skin Barrier Activity [PE]"], "manufacturer_name": ["Infirst Healthcare Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "355 mL in 1 BOTTLE, PLASTIC (62372-504-12)", "package_ndc": "62372-504-12", "marketing_start_date": "20160321"}], "brand_name": "Mylanta Maximum Strength Vanilla Caramel Flavor", "product_id": "62372-504_0bb0df3b-05ce-5c5b-e063-6394a90ab91a", "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": "62372-504", "generic_name": "Antacid and Anti Gas Aluminum hydroxide Magnesium hydroxide and Simethicone", "labeler_name": "Infirst Healthcare Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mylanta Maximum Strength Vanilla Caramel Flavor", "active_ingredients": [{"name": "ALUMINUM HYDROXIDE", "strength": "800 mg/10mL"}, {"name": "DIMETHICONE", "strength": "80 mg/10mL"}, {"name": "MAGNESIUM HYDROXIDE", "strength": "800 mg/10mL"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20160321", "listing_expiration_date": "20261231"}