Class II · Moderate risk
Fluocinonide
Failed Viscosity Specifications: Out of Specification results, above the specification limit, in viscosity, noted during stability testing.
National Drug Code
Is NDC 51672-1386-02 recalled?
Fluocinonide · 1 TUBE in 1 CARTON (51672-1386-2) / 30 g in 1 TUBE
Yes — this exact package was recalled
1 FDA recall names the code 51672-1386-02 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.
3 of these recalls are still ongoing.
- Active ingredient
- Fluocinonide
- Strength
- FLUOCINONIDE .5 mg/g
- Form
- Cream · Topical
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Type
- Human Prescription Drug
- Product code
- 51672-1386
Recalls naming this package
Class II · Moderate risk
Fluocinonide
Failed Viscosity Specifications: Out of Specification results, above the specification limit, in viscosity, noted during stability testing.
Class II · Moderate risk
Fluocinonide
Failed Viscosity Specifications: Out of Specification results, above the specification limit, in viscosity, noted during stability testing.
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
- 51672-1351 Ciclopirox 2
- 51672-1385 Ibuprofen 2
- 51672-2130 Ibuprofen 2
- 51672-3007 Hydrocortisone and Acetic Acid 2
- 51672-4005 Carbamazepine 2
- 51672-4027 Warfarin Sodium 2
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