mintox maximum strength

Generic: aluminum hydroxide, magnesium hydroxide, dimethicone

Labeler: atlantic biologicals corp.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name mintox maximum strength
Generic Name aluminum hydroxide, magnesium hydroxide, dimethicone
Labeler atlantic biologicals corp.
Dosage Form SUSPENSION
Routes
ORAL
Active Ingredients

aluminum hydroxide 400 mg/5mL, dimethicone 40 mg/5mL, magnesium hydroxide 400 mg/5mL

Manufacturer
ATLANTIC BIOLOGICALS CORP.

Identifiers & Regulatory

Product NDC 17856-5725
Product ID 17856-5725_3b3f429e-d2e4-441c-e063-6294a90aaf4d
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M
Listing Expiration 2026-12-31
Marketing Start 2011-02-01

Pharmacologic Class

Physiologic Effect
skin barrier activity [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 178565725
Hyphenated Format 17856-5725

Supplemental Identifiers

RxCUI
237870 708127
UNII
5QB0T2IUN0 92RU3N3Y1O NBZ3QY004S
NUI
N0000010282

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 M (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 400 mg/5mL
  • 40 mg/5mL
source: ndc
Packaging
  • 30 mL in 1 CUP (17856-5725-3)
source: ndc

Packages (1)

Ingredients (3)

aluminum hydroxide (400 mg/5mL) dimethicone (40 mg/5mL) magnesium hydroxide (400 mg/5mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3b3f429e-d2e4-441c-e063-6294a90aaf4d", "openfda": {"nui": ["N0000010282"], "unii": ["5QB0T2IUN0", "92RU3N3Y1O", "NBZ3QY004S"], "rxcui": ["237870", "708127"], "spl_set_id": ["ac6a47e7-972f-4b82-96da-89926d345e9f"], "pharm_class_pe": ["Skin Barrier Activity [PE]"], "manufacturer_name": ["ATLANTIC BIOLOGICALS CORP."]}, "finished": true, "packaging": [{"sample": false, "description": "30 mL in 1 CUP (17856-5725-3)", "package_ndc": "17856-5725-3", "marketing_start_date": "20210128"}], "brand_name": "MINTOX MAXIMUM STRENGTH", "product_id": "17856-5725_3b3f429e-d2e4-441c-e063-6294a90aaf4d", "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": "17856-5725", "generic_name": "aluminum hydroxide, magnesium hydroxide, dimethicone", "labeler_name": "ATLANTIC BIOLOGICALS CORP.", "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": "M", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20110201", "listing_expiration_date": "20261231"}