Class II · Moderate risk
Dry Eye Relief Lubricant Eye Drops
CGMP Deviations: good manufacturing deficiencies related to a lack of documentation of the fill line.
National Drug Code
Is NDC 49035-0280-02 recalled?
Equate Eye Drops Dry Eye Relief · 2 BOTTLE, DROPPER in 1 BOX (49035-280-02) / 15 mL in 1 BOTTLE, DROPPER
Yes — this exact package was recalled
1 FDA recall names the code 49035-0280-02 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
- Wal-Mart Stores, Inc.
- Type
- Human OTC Drug
- Product code
- 49035-0280
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
- 49035-0882 See recall 3
- 49035-0125 See recall 2
- 49035-0229 Acne Treatment 2
- 49035-0273 See recall 2
- 49035-0313 Equate Childrens Pain and Fever 2
- 49035-0404 See recall 2
Free recall alerts
Know the day your medication is recalled
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