Class II · Moderate risk
PureLife
Defective container:may contain bottles with incomplete seals
National Drug Code
Is NDC 68987-0001-30 recalled?
PureLife Topical Anesthetic · 30 g in 1 JAR (68987-001-30)
Yes — this exact package was recalled
1 FDA recall names the code 68987-0001-30 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
- Benzocaine
- Strength
- BENZOCAINE 200 mg/g
- Form
- Gel · Dental
- Labeler
- PureLife Dental
- Type
- Human OTC Drug
- Product code
- 68987-0001
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.
Free recall alerts
Know the day your medication is recalled
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