Always Be Clean Hand Sanitizer

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

Why it was recalled

Labeling Not Elsewhere Classified: Product labeled to contain methanol

Wrong label, wrong strength, mixed-up products, or packaging errors. One of the most dangerous causes - you can end up taking the wrong drug or the wrong dose. All labeling / mix-up recalls.

What was recalled

Always Be Clean Hand Sanitizer (73% Alcohol) 0.04 FL OZ (1.2 mL) packaged in a) Single snaps (NDC 75091-2020-1 UPC 375091202016); b) 100-count boxes (NDC 75091-2020-2 UPC 375091202023); c) 25-count boxes (NDC 75091-2020-3 UPC 375091202030)

Affected NDCs 75091-2020-01 75091-2020-02 75091-2020-03

Compare with the code on your package — it is the most precise check available.

Drug: Alcohol

Recalling firm: Open Book Extracts
NDC code: 75091-2020-1
Origin: NC, United States
Initiated by: Voluntary: Firm initiated
Company announcement: Aug 29, 2020 · FDA notice with lot numbers
FDA recall number: D-1563-2020 · 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.