inon ace
Generic: magnesium aluminosilicates, magnesium hydroxide, simethicone
Labeler: sato pharmaceutical co., ltd.Drug Facts
Product Profile
Brand Name
inon ace
Generic Name
magnesium aluminosilicates, magnesium hydroxide, simethicone
Labeler
sato pharmaceutical co., ltd.
Dosage Form
TABLET
Routes
Active Ingredients
dimethicone 20 mg/1, magnesium hydroxide 60 mg/1, silodrate 200 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
49873-402
Product ID
49873-402_09d87d9c-fe4c-fd02-e063-6394a90a56bd
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M001
Listing Expiration
2026-12-31
Marketing Start
1995-11-01
Pharmacologic Class
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
49873402
Hyphenated Format
49873-402
Supplemental Identifiers
RxCUI
UPC
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
inon ace (source: ndc)
Generic Name
magnesium aluminosilicates, magnesium hydroxide, simethicone (source: ndc)
Application Number
M001 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/1
- 60 mg/1
- 200 mg/1
Packaging
- 1 BOTTLE in 1 CARTON (49873-402-01) / 75 TABLET in 1 BOTTLE
Packages (1)
Ingredients (3)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "09d87d9c-fe4c-fd02-e063-6394a90a56bd", "openfda": {"nui": ["N0000010282"], "upc": ["0349873402017"], "unii": ["92RU3N3Y1O", "NBZ3QY004S", "9T3UU8T0QK"], "rxcui": ["1235450", "1235456"], "spl_set_id": ["0af4355f-e160-409d-8471-2de98dbc6f7c"], "pharm_class_pe": ["Skin Barrier Activity [PE]"], "manufacturer_name": ["Sato Pharmaceutical Co., Ltd."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (49873-402-01) / 75 TABLET in 1 BOTTLE", "package_ndc": "49873-402-01", "marketing_start_date": "19951101"}], "brand_name": "Inon Ace", "product_id": "49873-402_09d87d9c-fe4c-fd02-e063-6394a90a56bd", "dosage_form": "TABLET", "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": "49873-402", "generic_name": "magnesium aluminosilicates, magnesium hydroxide, simethicone", "labeler_name": "Sato Pharmaceutical Co., Ltd.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Inon Ace", "active_ingredients": [{"name": "DIMETHICONE", "strength": "20 mg/1"}, {"name": "MAGNESIUM HYDROXIDE", "strength": "60 mg/1"}, {"name": "SILODRATE", "strength": "200 mg/1"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "19951101", "listing_expiration_date": "20261231"}