Class II · Moderate risk
Vista Gonio Eye Lubricant
Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.
National Drug Code
Is NDC 77790-0022-15 recalled?
Vista Gonio Eye Lubricant · 1 BOTTLE, DROPPER in 1 CARTON (77790-022-15) / 15 mL in 1 BOTTLE, DROPPER
Yes — this exact package was recalled
1 FDA recall names the code 77790-0022-15 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
- Hypromellose Ophthalmic Solution
- Strength
- HYPROMELLOSE 2208 (100 MPA.S) 25 mg/15mL
- Form
- Solution · Ophthalmic
- Labeler
- Red Wedding LLC
- Type
- Human OTC Drug
- Product code
- 77790-0022
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
- 77790-0001 See recall 1
- 77790-0002 VISTA Hypromellose Dry Eye Relief 1
- 77790-0003 VISTA MEIBO TEARS Propylene Glycol 0.6% w/v Advanced Dry Eye Relief Lubricating Drops 10 ml 1
Free recall alerts
Know the day your medication is recalled
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