Class II · Moderate risk
Triamcinolone Acetonide cream
cGMP deviations: Temperature abuse
National Drug Code
Is NDC 0168-0004-15 recalled?
triamcinolone acetonide · 1 TUBE in 1 CARTON (0168-0004-15) / 15 g in 1 TUBE
Yes — this exact package was recalled
1 FDA recall names the code 0168-0004-15 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.
- Active ingredient
- triamcinolone acetonide
- Strength
- TRIAMCINOLONE ACETONIDE 1 mg/g
- Form
- Cream · Topical
- Labeler
- E. Fougera & Co. a division of Fougera Pharmaceuticals, LLC
- Type
- Human Prescription Drug
- Product code
- 0168-0004
Recalls naming this package
Class III · Low risk
Triamcinolone Acetonide Cream USP
Labeling: Label Error on Declared Strength: There is a misprint on the end flap which read 01% rather than 0.1%.
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
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