Class II · Moderate risk
Eyesaline
CGMP Deviations
National Drug Code
Is NDC 0498-0631-37 recalled?
Fendall 2000 Pure Flow · 29.9 L in 1 CONTAINER (0498-0631-37)
Yes — this exact package was recalled
1 FDA recall names the code 0498-0631-37 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.
- Active ingredient
- Purified water
- Strength
- WATER 98.6 L/100L
- Form
- Liquid · Ophthalmic
- Labeler
- Honeywell Safety Products USA, Inc.
- Type
- Human OTC Drug
- Product code
- 0498-0631
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
- 0498-0750 See recall 1
Free recall alerts
Know the day your medication is recalled
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