FDA DrugsClass II
PureLife, TOPICAL ANESTHETIC GEL, BENZOCAINE 20%, 1 oz (30mL), Strawberry Flavo...
Published: June 24, 2026Recall ID: D-0605-2026Category: drugsCountry: US
Reason for Recall / Hazard
Defective container:may contain bottles with incomplete seals
Product Description & Identification
PureLife, 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
Affected Products
PureLife, 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
Additional Source Details
| Field | Value |
|---|---|
| City | Gibbstown |
| State | NJ |
| Openfda › Nui › 1 | N0000185508 |
| Openfda › Nui › 2 | N0000175629 |
| Openfda › Nui › 3 | N0000184306 |
| Openfda › Nui › 4 | M0000728 |
| Openfda › Unii | U3RSY48JW5 |
| Openfda › Route | DENTAL |
| Openfda › Rxcui | 238910 |
| Openfda › Spl id | 2b386f93-586f-d4aa-e063-6394a90a4a47 |
| Openfda › Brand name | PURELIFE TOPICAL ANESTHETIC |
| Openfda › Spl set id | 4e68a4b9-a08c-4360-92b7-53d0f9df092d |
| Openfda › Package ndc | 68987-001-30 |
| Openfda › Product ndc | 68987-001 |
| Openfda › Generic name | BENZOCAINE |
| Openfda › Product type | HUMAN OTC DRUG |
| Openfda › Pharm class cs | Allergens [CS] |
| Openfda › Pharm class pe › 1 | Increased Histamine Release [PE] |
| Openfda › Pharm class pe › 2 | Cell-mediated Immunity [PE] |
| Openfda › Substance name | BENZOCAINE |
| Openfda › Pharm class epc | Standardized Chemical Allergen [EPC] |
| Openfda › Manufacturer name | PureLife Dental |
| Openfda › Application number | M022 |
| Openfda › Is original packager | true |
| Event id | 99076 |
| Address 1 | 480 S Democrat Rd |
| Code info | BNZ-001921, EXP 04/15/2029 |
| Postal code | 08027-1239 |
| Report date | 20260624 |
| Product type | Drugs |
| Product quantity | 450 units |
| Reason for recall | Defective container:may contain bottles with incomplete seals |
| Voluntary mandated | Voluntary: Firm initiated |
| Recall initiation date | 20260521 |
| Initial firm notification | Letter |
| Center classification date | 20260618 |
Overview
- Recalling FirmKeystone Industries
- StatusOngoing
- Risk LevelClass II
- DistributionNationwide in the USA