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Class II · ModerateActive recall

Purelife Topical Anesthetic

Could cause temporary or reversible harm; serious harm is unlikely.

Does this affect you?
Check your lot numberBNZ-001921, EXP 04/15/2029
Where it was soldNationwide in the USA
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.

What happened

Defective container:may contain bottles with incomplete seals

What to do

  1. Check the lot number and expiry on your medicine against the recall above.
  2. Talk to your pharmacist or doctor before changing anything — don't stop on your own.
  3. Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).

Who makes it

Made byPureLife Dental
Brand namePURELIFE TOPICAL ANESTHETIC
Generic nameBENZOCAINE
Active ingredient(s)BENZOCAINE
Distributed by / forPure Life, LLC, Manufactured for PureLife LLC., Carson, CA 90810
NDC68987-001-30
Show the full FDA record
Full product labelPureLife, TOPICAL ANESTHETIC GEL, BENZOCAINE 20%, 1 oz (30mL), Strawberry Flavor, Manufactured for Pure Life, LLC, Manufactured for PureLife LLC., Carson, CA 90810. NDC 68987-001-30
Recalling firmKeystone Industries
DistributionNationwide in the USA
Quantity450 units
Recall initiated2026-05-21
Report date2026-06-24
Recall completed—
Recall numberD-0605-2026
ClassificationClass II
FDA statusOngoing
Origin on fileGibbstown NJ United States

Related

Recent drug recallsCheck another medication

Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗

This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.