mintox maximum strength

Generic: aluminum hydroxide, magnesium hydroxide, dimethicone

Labeler: proficient rx lp
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 proficient rx lp
Dosage Form SUSPENSION
Routes
ORAL
Active Ingredients

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

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-515
Product ID 71205-515_dddf9006-4715-487a-b12f-67d56a9e1993
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
skin barrier activity [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71205515
Hyphenated Format 71205-515

Supplemental Identifiers

RxCUI
237870 708127
UPC
0371205515355
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 M001 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 400 mg/5mL
  • 40 mg/5mL
source: ndc
Packaging
  • 355 mL in 1 BOTTLE (71205-515-35)
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": "dddf9006-4715-487a-b12f-67d56a9e1993", "openfda": {"nui": ["N0000010282"], "upc": ["0371205515355"], "unii": ["5QB0T2IUN0", "92RU3N3Y1O", "NBZ3QY004S"], "rxcui": ["237870", "708127"], "spl_set_id": ["b7711b50-c14a-44d6-b647-1f31284f87ea"], "pharm_class_pe": ["Skin Barrier Activity [PE]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "355 mL in 1 BOTTLE (71205-515-35)", "package_ndc": "71205-515-35", "marketing_start_date": "20201216"}], "brand_name": "MINTOX MAXIMUM STRENGTH", "product_id": "71205-515_dddf9006-4715-487a-b12f-67d56a9e1993", "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": "71205-515", "generic_name": "aluminum hydroxide, magnesium hydroxide, dimethicone", "labeler_name": "Proficient Rx LP", "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"}