Class II ยท Moderate risk
Muro 128 (sodium chloride)
Crystallization: Crystal precipitate formation and an increase in the number of complaints associated with a gritty, sand-like feeling in the eye.
National Drug Code
Is NDC 24208-0385-01 recalled?
Muro 128 · 1 TUBE in 1 CARTON (24208-385-01) / 1 g in 1 TUBE
Yes — this exact package was recalled
1 FDA recall names the code 24208-0385-01 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.
- Active ingredient
- sodium chloride
- Strength
- SODIUM CHLORIDE 50 mg/g
- Form
- Ointment · Ophthalmic
- Labeler
- Bausch & Lomb Incorporated
- Type
- Human OTC Drug
- Product code
- 24208-0385
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
- 24208-0280 See recall 1
- 24208-0439 See recall 1
- 24208-0503 Lotemax 1
- 24208-0507 Lotemax SM 1
- 24208-0539 Miochol E 1
- 24208-0585 Tropicamide 1
Free recall alerts
Know the day your medication is recalled
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