Class III ยท Low risk
Dibucaine 1% Hemorrhoidal Ointment
Labeling: Incorrect or Missing Lot and/or Exp Date
National Drug Code
Is NDC 71399-2829-01 recalled?
Dibucaine · 28 g in 1 TUBE (71399-2829-1)
Yes — this exact package was recalled
1 FDA recall names the code 71399-2829-01 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
- Dibucaine
- Strength
- DIBUCAINE .28 g/28g
- Form
- Ointment · Topical
- Labeler
- Akron Pharma Inc.
- Type
- Human OTC Drug
- Product code
- 71399-2829
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
- 71399-8022 See recall 3
- 71399-8024 See recall 2
- 71399-8028 See recall 2
- 71399-0039 See recall 1
- 71399-8014 See recall 1
- 71399-8026 See recall 1
Free recall alerts
Know the day your medication is recalled
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