Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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Class II · Moderate risk Terminated Initiated Oct 9, 2018 (8 years ago)

Body Skin Tonic

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

Why it was recalled

CGMP Deviations: products manufactured by contract manufacturer under conditions that could result in possible microbial contamination.

Cause type: Microbial contamination

Bacteria, mold, yeast or other microorganisms detected in the product. Contamination can occur from water systems, equipment or handling, and can cause infection. All microbial contamination recalls.

What was recalled

Body Skin Tonic, Homeopathic Oral Spray 1.38 fl. oz. (41 mL). Manufactured by Sprayology Gaithersburg, MD 20879. NDC 61096-0017-1

Affected NDC 61096-0017-01

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

Recalling firm
Sprayology
NDC code
61096-0017-1
Origin
MD, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0123-2019 · 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.

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All 2018 recalls
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Terminated Microbial contamination Sprayology NDC 61096-0004-1 D-0126-2019
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CGMP Deviations: products manufactured by contract manufacturer under conditions that could result in possible microbial contamination.

Terminated Microbial contamination Sprayology NDC 61096-0038-1 D-0122-2019

Other microbial contamination recalls from 2018

All microbial contamination recalls