Class II · Moderate risk
Dry Eye Relief Eye Drops
Lack of Assurance of Sterility
National Drug Code
Is NDC 70000-0502-01 recalled?
Leader Dry Eye Relief Eye Drops · 1 BOTTLE, PLASTIC in 1 CARTON (70000-0502-1) / 15 mL in 1 BOTTLE, PLASTIC
Yes — this exact package was recalled
1 FDA recall names the code 70000-0502-01 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
- Glycerin, Hypromellose, Polyethylene glycol 400
- Strength
- GLYCERIN .2 g/100mL; HYPROMELLOSE, UNSPECIFIED .2 g/100mL…
- Form
- Solution/ Drops · Ophthalmic
- Labeler
- Cardinal Health 110, LLC. Dba Leader
- Type
- Human OTC Drug
- Product code
- 70000-0502
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
- 70000-0090 Lubricant Drops 3
- 70000-0087 Eyes Irritation Relief 2
- 70000-0088 Dry eye relief 2
- 70000-0089 Dry Eye Relief 2
- 70000-0454 See recall 2
- 70000-0518 See recall 2
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