aluminum hydroxide, magnesium hydroxide, and dimethicone
Generic: aluminum hydroxide, magnesium hydroxide, and dimethicone
Labeler: american health packagingDrug Facts
Product Profile
Brand Name
aluminum hydroxide, magnesium hydroxide, and dimethicone
Generic Name
aluminum hydroxide, magnesium hydroxide, and dimethicone
Labeler
american health packaging
Dosage Form
SUSPENSION
Routes
Active Ingredients
aluminum hydroxide 400 mg/5mL, dimethicone, unspecified 40 mg/5mL, magnesium hydroxide 400 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
60687-888
Product ID
60687-888_39fbaa0c-00d4-898a-e063-6394a90a5a7e
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M002
Listing Expiration
2026-12-31
Marketing Start
2025-07-15
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
60687888
Hyphenated Format
60687-888
Supplemental Identifiers
RxCUI
UNII
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
aluminum hydroxide, magnesium hydroxide, and dimethicone (source: ndc)
Generic Name
aluminum hydroxide, magnesium hydroxide, and dimethicone (source: ndc)
Application Number
M002 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 400 mg/5mL
- 40 mg/5mL
Packaging
- 10 TRAY in 1 CASE (60687-888-76) / 10 CUP, UNIT-DOSE in 1 TRAY (60687-888-51) / 30 mL in 1 CUP, UNIT-DOSE (60687-888-45)
Packages (1)
Ingredients (3)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "39fbaa0c-00d4-898a-e063-6394a90a5a7e", "openfda": {"unii": ["5QB0T2IUN0", "92RU3N3Y1O", "NBZ3QY004S"], "rxcui": ["237870"], "spl_set_id": ["23539e7e-a723-460f-892f-dac5bbbb9b16"], "manufacturer_name": ["American Health Packaging"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 TRAY in 1 CASE (60687-888-76) / 10 CUP, UNIT-DOSE in 1 TRAY (60687-888-51) / 30 mL in 1 CUP, UNIT-DOSE (60687-888-45)", "package_ndc": "60687-888-76", "marketing_start_date": "20250715"}], "brand_name": "Aluminum Hydroxide, Magnesium Hydroxide, and Dimethicone", "product_id": "60687-888_39fbaa0c-00d4-898a-e063-6394a90a5a7e", "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": "60687-888", "generic_name": "Aluminum Hydroxide, Magnesium Hydroxide, and Dimethicone", "labeler_name": "American Health Packaging", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Aluminum Hydroxide, Magnesium Hydroxide, and Dimethicone", "active_ingredients": [{"name": "ALUMINUM HYDROXIDE", "strength": "400 mg/5mL"}, {"name": "DIMETHICONE, UNSPECIFIED", "strength": "40 mg/5mL"}, {"name": "MAGNESIUM HYDROXIDE", "strength": "400 mg/5mL"}], "application_number": "M002", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250715", "listing_expiration_date": "20261231"}