Petroleum Jelly
FDA Recall NDC 72036-069
FDA Enforcement Report: View Recall Date, Reasons, and Safety Status
Active & Historical Enforcement Reports
The FDA has identified 1 recorded enforcement report(s) associated with Petroleum (NDC 72036-069). A significant event, classified as Class II, was initiated on May 28, 2024 by Harris Teeter. The reported reason for this action was: "Labeling: Label Mix up; product labeled as pure white petroleum jelly actually contains petroleum jelly with Lavendar and Chamomile"
This specific recall has a current status of TERMINATED, indicating that the FDA considers the recall process finished or the product successfully recovered.
This specific recall has a current status of TERMINATED, indicating that the FDA considers the recall process finished or the product successfully recovered.
Reported Recall Events
Class II Terminated
Labeling: Label Mix up; product labeled as pure white petroleum jelly actually contains petroleum jelly with Lavendar and Chamomile
May 28, 2024
Jun 26, 2024
1015 cases
Recall Profile & Regulatory Data
Event ID
94710
Classification
Class II
Enforcement Status
Terminated
Recalling Firm
Consumer Product Partners, LLC
Voluntary / Mandated
Voluntary: Firm initiated
Distribution Pattern
Nationwide.
Termination Date
Aug 21, 2025
Product Description
Petroleum Jelly, White Petrolatum USP, NET WT 13 OZ (368g), sold under the following brands - Rite Aid, with UPC 0-11822-51349-4; Kroger, with UPC 0-41260-35275-1; Harris Teeter, with UPC 0-72036-75051-8; CVS, with UPC 0-50428-31702-0
Batch or Lot Expiration Information
Lot# Rite Aid -
Lot# 0607983, expiration date: 07/2026, NDC # 11822-3135-2 Kroger-
Lot# 0607983, expiration date: 07/2026, NDC# 30142-069-27 Harris Teeter -
Lot# 0607983, expiration date: 07/2026, NDC# 72036-069-27 CVS-
Lot# 0607983, expiration date: 07/2026, NDC # 59779-069-27
Affected Packages Involved in this Recall
11822-3135-4Product
11822-3135-2Product
30142-069-07Product
30142-069-27Product
30142-069-54Product
72036-069-27Product
72036-069-54Product
59779-069-27Product
59779-069-54Product
59779-069-18Product
59779-069-96Product
About FDA Recall Enforcement Reports
FDA recall data documents classified recall actions associated with a product. Most recalls are limited to specific lots, batches, or package configurations rather than every unit of a drug.
If a recall is listed for an NDC, review the affected lot information and package details carefully. Patients and healthcare professionals should confirm whether a specific product in hand matches the lot or package information before assuming it is affected.
