Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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National Drug Code

Is NDC 43386-0069-60 recalled?

Fluocinolone Acetonide · 1 BOTTLE in 1 CARTON (43386-069-60) / 60 mL in 1 BOTTLE

Yes — this exact package was recalled

3 FDA recalls name the code 43386-0069-60 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
Fluocinolone Acetonide
Strength
FLUOCINOLONE ACETONIDE .1 mg/mL
Form
Solution · Topical
Labeler
Lupin Pharmaceuticals,Inc.
Type
Human Prescription Drug
Product code
43386-0069

Recalls naming this package

Class II · Moderate risk

Fluocinolone Acetonide Topical Solution

Failed Impurities/Degradation Specifications: Expansion of October 2018 recall due to elevated out of specification results for total impurities that have been chemically identified as oxidative degradation products of the fluocinolone active pharmaceutical ingredient.

Terminated Impurity / degradation Lupin Somerset NDC 43386-069-60 D-0390-2019

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