Good Neighbor Pharmacy Alcohol Antiseptic Skin Cleanser Swab
FDA Recall NDC 46122-043
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 Good Neighbor Pharmacy Alcohol Antiseptic Skin Cleanser (NDC 46122-043). A significant event, classified as Class II, was initiated on Jul 07, 2025 by Amerisouce Bergen. The reported reason for this action was: "Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration."
This recall is currently ONGOING. Healthcare providers and patients are advised to check their inventory immediately against the affected codes provided below.
This recall is currently ONGOING. Healthcare providers and patients are advised to check their inventory immediately against the affected codes provided below.
Reported Recall Events
July 2025 Class II Recall: Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration.
Recall Number
Class II Ongoing
Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration.
Jul 07, 2025
Sep 03, 2025
66,000 pads
Recall Profile & Regulatory Data
Event ID
97385
Classification
Class II
Enforcement Status
Ongoing
Recalling Firm
MEDLINE INDUSTRIES, LP - Northfield
Voluntary / Mandated
Voluntary: Firm initiated
Distribution Pattern
Nationwide
Product Description
Good Neighbor Pharmacy, Alcohol Prep Pads, Distributed By AmeriSource Bergen, 1 West First Avenue, Conshohocken, PA 19428, Made in China: 100 eaches per box, 30 boxes per case, (3,000 eaches per case), NDC 46122-043-78.
Batch or Lot Expiration Information
Lot# 61224070074
Affected Packages Involved in this Recall
46122-043-78Product
6122407007Product
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.
