Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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Class II · Moderate risk Terminated Initiated Dec 7, 2017 (9 years ago)

Neutrogena Acne Proofing whipped foam cleanser

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Defective Container: products showed leakage (bubbles, foaming) of propellant and product from the container valve cup area.

Cause type: Packaging defect

Failed child-resistant closures, leaks, cracked containers, or a defective delivery device. Packaging failures risk accidental exposure (especially to children) or product contamination. All packaging defect recalls.

What was recalled

Neutrogena Acne Proofing whipped foam cleanser, (Salicylic Acid 2%), aerosolized product in a can, NET WT. 5 OZ (141 g) , Distributed by Johnson & Johnson Consumer Inc. Skillman, NJ 08558, UPC 0 70501 11131 4

Recalling firm
Johnson & Johnson
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0243-2018 · FDA notice

Check, then ask. Class II means harm is possible but usually temporary or reversible. Find the lot number on your package; if it matches, ask your pharmacist about a replacement. Do not simply stop a prescribed medication on your own - the gap can be riskier than the recall. This recall is now terminated, which means the firm has finished removing the affected product; anything on pharmacy shelves today should be unaffected.

Other recalls by Johnson & Johnson

All 2017 recalls
Class II · Moderate risk

Neutrogena Elevated 4-Holiday Trays

Defective Container: products showed leakage (bubbles, foaming) of propellant and product from the container valve cup area.

Terminated Packaging defect Johnson & Johnson D-0245-2018

Other packaging defect recalls from 2017

All packaging defect recalls
Class II · Moderate risk

Neutrogena Elevated 4-Holiday Trays

Defective Container: products showed leakage (bubbles, foaming) of propellant and product from the container valve cup area.

Terminated Packaging defect Johnson & Johnson D-0245-2018