NDC 49873-402

Inon Ace

Magnesium Aluminosilicates, Magnesium Hydroxide, Simethicone

Inon Ace is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Sato Pharmaceutical Co., Ltd.. The primary component is Magnesium Hydroxide; Silodrate; Dimethicone.

• Product ID: 49873-402_99f61abf-f0ba-f7aa-e053-2a95a90a3b32
• NDC: 49873-402
• Product Type: Human Otc Drug
• Proprietary Name: Inon Ace
• Generic Name: Magnesium Aluminosilicates, Magnesium Hydroxide, Simethicone
• Dosage Form: Tablet
• Route of Administration: ORAL
• Marketing Start Date: 1995-11-01
• Marketing Category: OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
• Application Number: part331
• Labeler Name: Sato Pharmaceutical Co., Ltd.
• Substance Name: MAGNESIUM HYDROXIDE; SILODRATE; DIMETHICONE
• Active Ingredient Strength: 60 mg/1; mg/1; mg/1
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 49873-402-01

1 BOTTLE in 1 CARTON (49873-402-01) > 75 TABLET in 1 BOTTLE

• Marketing Start Date: 1995-11-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 49873-402-01 [49873040201]

Inon Ace TABLET

• Marketing Category: OTC monograph final
• Application Number: part331
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 1995-11-01

Drug Details

Active Ingredients

Ingredient	Strength
MAGNESIUM HYDROXIDE	60 mg/1

OpenFDA Data

• SPL SET ID: 0af4355f-e160-409d-8471-2de98dbc6f7c
• Manufacturer:
  • Sato Pharmaceutical Co., Ltd.
• UNII:
  • 9T3UU8T0QK
  • NBZ3QY004S
  • 92RU3N3Y1O
• RxNorm Concept Unique ID - RxCUI:
  • 1235450
  • 1235456
• UPC Code:
  • 0349873402017

NDC Crossover Matching brand name "Inon Ace" or generic name "Magnesium Aluminosilicates, Magnesium Hydroxide, Simethicone"

NDC	Brand Name	Generic Name
49873-402	Inon Ace	magnesium aluminosilicates, magnesium hydroxide, simethicone
49873-403	Inon Ace	magnesium aluminosilicate, magnesium hydroxide