Class III ยท Low risk
Diflorasone Diacetate Ointment
Failed Impurities/Degradation Specifications: The impurity results at 12 months stability testing,did not conform to the specification limit.
National Drug Code
Is NDC 64980-0124-60 recalled?
Diflorasone Diacetate · 1 TUBE in 1 CARTON (64980-124-60) / 60 g in 1 TUBE
Yes — this exact package was recalled
1 FDA recall names the code 64980-0124-60 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.
1 of these recalls is still ongoing.
- Active ingredient
- diflorasone diacetate
- Strength
- DIFLORASONE DIACETATE .5 mg/g
- Form
- Ointment · Topical
- Labeler
- Rising Pharma Holdings, Inc.
- Type
- Human Prescription Drug
- Product code
- 64980-0124
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
- 64980-0514 Timolol Maleate 8
- 64980-0504 Cyproheptadine Hydrochloride 2
- 64980-0513 Timolol Maleate 2
- 64980-0599 Chlorthalidone 2
- 64980-0104 Dibasic Sodium Phosphate, Monobasic Potassium Phosphate and Monobasic Sodium Phosphate 1
- 64980-0129 See recall 1
Free recall alerts
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