CLASS II ONGOING Drug recall · Reported 10 Jul 2024 · FDA Enforcement Report
Clear Breeze Plus, Hand Sanitizer recalled by Little Moon Essentials
Little Moon Essentials is recalling Clear Breeze Plus, Hand Sanitizer (Alcohol 65% v/v) Packaged as a) spray, distributed nationwide in the US. The recall was initiated on 20 Jun 2024 and the FDA has classified it as Class II.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-0578-2024
- FDA event ID
- 94788
- Recalling firm
- Little Moon Essentials, Dania Beach, FL
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 20 Jun 2024
- FDA classified
- 2 Jul 2024
- Reported
- 10 Jul 2024
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Manufacturing (CGMP) Deviations
- Drug class
- Hand Sanitizer
Timeline
| 20 Jun 2024 | Recall initiated by company | |
| 2 Jul 2024 | Classified by FDA | +12 days |
| 10 Jul 2024 | Published in enforcement report | +8 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
CGMP deviations
Product as listed by the FDA
Little Moon Essentials, Clear Breeze Plus, Hand Sanitizer (Alcohol 65% v/v) Packaged as a) 2 FL OZ (60ML) spray bottle, UPC Code 6 73673 88797 3, NDC 70722-319-02; b) 4 FL OZ (118ML) spray bottle, UPC Code 6 73673 88798 0, NDC 70722-319-04; Little Moon Essentials LLC Dania Beach, Fl 33004
Where it was distributed
Nationwide USA and Ontario, Canada (2 retailers)
Questions about this recall
Why was it recalled?
CGMP deviations
Which lots are affected?
lot code expiration dates are not on products: a) 023170, b) 023170
Where was it sold?
Nationwide USA and Ontario, Canada (2 retailers)
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other products in this recall event
7 other products · FDA event 94788This product is part of a recall event; the main page for the event is Crampy Belly Rub (Camphor 1.1%), Packaged as a) recalled.