Class II · Moderate risk
Ultra Lubricating Eye Drops
Lack of Assurance of Sterility
National Drug Code
Is NDC 50804-0160-01 recalled?
GoodSense Ultra Lubricant Eye Drops · 1 BOTTLE, DROPPER in 1 CARTON (50804-160-01) / 15 mL in 1 BOTTLE, DROPPER
Yes — this exact package was recalled
2 FDA recalls name the code 50804-0160-01 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
- polyethylene glycol 400, propylene glycol
- Strength
- PROPYLENE GLYCOL .3 g/100mL; POLYETHYLENE GLYCOL 400 .4…
- Form
- Solution · Ophthalmic
- Labeler
- Geiss, Destin & Dunn, Inc.
- Type
- Human OTC Drug
- Product code
- 50804-0160
Recalls naming this package
Class II · Moderate risk
Sterile EYE DROPS AC
Lack of Assurance of Sterility
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
- 50804-0141 GoodSense Eye Drops Original Formula 2
- 50804-0110 Good Sense Artificial Tears 1
- 50804-0129 GoodSense Extra Strength Antacid 1
- 50804-0130 GoodSense Eye Drops Advanced Relief Moisturizer 1
- 50804-0164 citroma 1
- 50804-0166 citroma 1
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