Class II ยท Moderate risk
Triamcinolone Acetonide cream
CGMP Deviations: Product complaints reporting the product to have a gritty texture and lack of effectiveness.
National Drug Code
Is NDC 72189-0330-80 recalled?
Triamcinolone Acetonide · 80 g in 1 TUBE (72189-330-80)
Yes — this exact package was recalled
1 FDA recall names the code 72189-0330-80 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 cream
- Strength
- TRIAMCINOLONE ACETONIDE 1 mg/g
- Form
- Cream · Topical
- Labeler
- Direct Rx
- Type
- Human Prescription Drug
- Product code
- 72189-0330
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
- 72189-0364 Ropinirole 2
- 72189-0058 See recall 1
- 72189-0064 Metformin Hydrochloride Extended Release 1
- 72189-0076 See recall 1
- 72189-0121 See recall 1
- 72189-0167 Losartan Potassium and Hydrochlorothiazide 1
Free recall alerts
Know the day your medication is recalled
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