Class II · Moderate risk
EYE DROPS Advanced Relief
Lack of Assurance of Sterility
National Drug Code
Is NDC 50804-0130-01 recalled?
GoodSense Eye Drops Advanced Relief Moisturizer · 1 CARTON in 1 CARTON (50804-130-01) / 15 mL in 1 CARTON
Yes — this exact package was recalled
1 FDA recall names the code 50804-0130-01 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
- dextran, polyethylene glycol 400, povidone, tetrahydrozoline HCl
- Strength
- POLYETHYLENE GLYCOL 400 1 g/100mL; TETRAHYDROZOLINE…
- Form
- Solution · Ophthalmic
- Labeler
- Geiss, Derstin & Dunn, Inc.
- Type
- Human OTC Drug
- Product code
- 50804-0130
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
- 50804-0141 GoodSense Eye Drops Original Formula 2
- 50804-0160 GoodSense Ultra Lubricant Eye Drops 2
- 50804-0110 Good Sense Artificial Tears 1
- 50804-0129 GoodSense Extra Strength Antacid 1
- 50804-0164 citroma 1
- 50804-0166 citroma 1
Free recall alerts
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