Class II · Moderate risk
INON ACE Antacid tablets
Failed Disintegration Specifications: above the time expected.
National Drug Code
Is NDC 49873-0402-01 recalled?
Inon Ace · 1 BOTTLE in 1 CARTON (49873-402-01) / 75 TABLET in 1 BOTTLE
Yes — this exact package was recalled
1 FDA recall names the code 49873-0402-01 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
1 of these recalls is still ongoing.
- Active ingredient
- magnesium aluminosilicates, magnesium hydroxide, simethicone
- Strength
- MAGNESIUM HYDROXIDE 60 mg/1; SILODRATE 200 mg/1…
- Form
- Tablet · Oral
- Labeler
- Sato Pharmaceutical Co., Ltd.
- Type
- Human OTC Drug
- Product code
- 49873-0402
Recalls naming this package
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Other recalled products from this labeler
- 49873-0020 See recall 1
- 49873-0044 See recall 1
- 49873-0404 Sankaijo 1
- 49873-0501 See recall 1
- 49873-0803 See recall 1
Free recall alerts
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