inon ace

Generic: magnesium aluminosilicate, magnesium hydroxide

Labeler: sato pharmaceutical co., ltd.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name inon ace
Generic Name magnesium aluminosilicate, magnesium hydroxide
Labeler sato pharmaceutical co., ltd.
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

magnesium hydroxide 250 mg/30mL, silodrate 900 mg/30mL

Manufacturer
Sato Pharmaceutical Co., Ltd.

Identifiers & Regulatory

Product NDC 49873-403
Product ID 49873-403_0bde7bd2-8a69-57b4-e063-6394a90a00d2
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M001
Listing Expiration 2026-12-31
Marketing Start 2000-05-20

Pharmacologic Class

Classes
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] stimulation large intestine fluid/electrolyte secretion [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 49873403
Hyphenated Format 49873-403

Supplemental Identifiers

RxCUI
1246297 1246303
UPC
0349873403014
UNII
NBZ3QY004S 9T3UU8T0QK

Packaging Origin

Original Packager
true

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 aluminosilicate, magnesium hydroxide (source: ndc)
Application Number M001 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/30mL
  • 900 mg/30mL
source: ndc
Packaging
  • 2 BOTTLE in 1 CARTON (49873-403-01) / 30 mL in 1 BOTTLE
source: ndc

Packages (1)

49873-403-01 2 BOTTLE in 1 CARTON (49873-403-01) / 30 mL in 1 BOTTLE

Ingredients (2)

magnesium hydroxide (250 mg/30mL) silodrate (900 mg/30mL)

Linked Drug Pages (1)

Inon Ace ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0bde7bd2-8a69-57b4-e063-6394a90a00d2", "openfda": {"upc": ["0349873403014"], "unii": ["NBZ3QY004S", "9T3UU8T0QK"], "rxcui": ["1246297", "1246303"], "spl_set_id": ["a6e4475c-dfac-493c-b98a-21473e3b59d5"], "manufacturer_name": ["Sato Pharmaceutical Co., Ltd."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BOTTLE in 1 CARTON (49873-403-01)  / 30 mL in 1 BOTTLE", "package_ndc": "49873-403-01", "marketing_start_date": "20000520"}], "brand_name": "Inon Ace", "product_id": "49873-403_0bde7bd2-8a69-57b4-e063-6394a90a00d2", "dosage_form": "SOLUTION", "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]", "Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]"], "product_ndc": "49873-403", "generic_name": "magnesium aluminosilicate, magnesium hydroxide", "labeler_name": "Sato Pharmaceutical Co., Ltd.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Inon Ace", "active_ingredients": [{"name": "MAGNESIUM HYDROXIDE", "strength": "250 mg/30mL"}, {"name": "SILODRATE", "strength": "900 mg/30mL"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20000520", "listing_expiration_date": "20261231"}