mintox maximum strength
Generic: aluminum hydroxide, magnesium hydroxide, dimethicone
Labeler: major pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
mintox maximum strength
Generic Name
aluminum hydroxide, magnesium hydroxide, dimethicone
Labeler
major pharmaceuticals inc.
Dosage Form
SUSPENSION
Routes
Active Ingredients
aluminum hydroxide 400 mg/5mL, dimethicone 40 mg/5mL, magnesium hydroxide 400 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
0904-5725
Product ID
0904-5725_092ff042-828f-4851-e063-6394a90aade4
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M001
Listing Expiration
2026-12-31
Marketing Start
2011-02-01
Pharmacologic Class
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
09045725
Hyphenated Format
0904-5725
Supplemental Identifiers
RxCUI
UNII
NUI
Packaging Origin
Original Packager
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
mintox maximum strength (source: ndc)
Generic Name
aluminum hydroxide, magnesium hydroxide, dimethicone (source: ndc)
Application Number
M001 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 400 mg/5mL
- 40 mg/5mL
Packaging
- 355 mL in 1 BOTTLE (0904-5725-14)
Packages (1)
Ingredients (3)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "092ff042-828f-4851-e063-6394a90aade4", "openfda": {"nui": ["N0000010282"], "unii": ["5QB0T2IUN0", "92RU3N3Y1O", "NBZ3QY004S"], "rxcui": ["237870", "708127"], "spl_set_id": ["536b143d-a1d7-4972-a90b-248e41937070"], "pharm_class_pe": ["Skin Barrier Activity [PE]"], "manufacturer_name": ["MAJOR Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "355 mL in 1 BOTTLE (0904-5725-14)", "package_ndc": "0904-5725-14", "marketing_start_date": "20161101"}], "brand_name": "MINTOX MAXIMUM STRENGTH", "product_id": "0904-5725_092ff042-828f-4851-e063-6394a90aade4", "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": "0904-5725", "generic_name": "aluminum hydroxide, magnesium hydroxide, dimethicone", "labeler_name": "MAJOR Pharmaceuticals Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "MINTOX MAXIMUM STRENGTH", "active_ingredients": [{"name": "ALUMINUM HYDROXIDE", "strength": "400 mg/5mL"}, {"name": "DIMETHICONE", "strength": "40 mg/5mL"}, {"name": "MAGNESIUM HYDROXIDE", "strength": "400 mg/5mL"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20110201", "listing_expiration_date": "20261231"}