Class I · High risk
Leader brand Dry Eye Relief
Non-Sterility
National Drug Code
Is NDC 70000-0089-01 recalled?
Dry Eye Relief · 1 BOTTLE, DROPPER in 1 CARTON (70000-0089-1) / 15 mL in 1 BOTTLE, DROPPER
Yes — this exact package was recalled
2 FDA recalls name the code 70000-0089-01 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.
2 of these recalls are still ongoing.
- Active ingredient
- Carboxymethylcellulose sodium
- Strength
- CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED 10 mg/mL
- Form
- Gel · Ophthalmic
- Labeler
- Cardinal Health 110, LLC. Dba Leader
- Type
- Human OTC Drug
- Product code
- 70000-0089
Recalls naming this package
Class I · High risk
LEADER brand Dry Eye Relief
Non-Sterility: FDA found insanitary conditions and positive bacterial test results from environmental sampling at the manufacturing facility.
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
- 70000-0454 See recall 2
- 70000-0518 See recall 2
- 70000-0576 See recall 2
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