Class II · Moderate risk
Med Pride
CGMP Deviations; deficiencies observed during FDA inspection
Remedy Gel
Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.
Why it was recalled
Subpotent Drug
Cause type: Wrong potency / content
Sub- or super-potent product, or a failed content-uniformity / assay test. You may receive too little or too much active ingredient - a direct dosing risk. All wrong potency / content recalls.
What was recalled
Remedy Gel, hydrocortisone 1%, 30 mL/ 1 fl oz per bottle, Distributed By: glo Skin Beauty, Denver, CO 80216. NDC 66915-531-12; 66915-531-13
Affected NDCs
66915-0531-12
66915-0531-13
Compare with the code on your package — it is the most precise check available.
Drug: Hydrocortisone
- Recalling firm
- Island Kinetics, Inc. d.b.a. CoValence Laboratories
- NDC code
- 66915-531-12
- Origin
- AZ, United States
- Initiated by
- Voluntary: Firm initiated
- FDA recall number
- D-0480-2026 · FDA notice
Low risk, still worth a check. Class III means the product is unlikely to cause harm but breaks an FDA rule (often labeling). If your lot matches, your pharmacy will normally swap it; there is no need for alarm. This recall is now terminated, which means the firm has finished removing the affected product; anything on pharmacy shelves today should be unaffected.
Other Hydrocortisone recalls
See all
Class II · Moderate risk
Med Pride
CGMP Deviations; deficiencies observed during FDA inspection
Class III · Low risk
Essential Calming Skin Gel
Subpotent Drug
Class III · Low risk
Skin Rehab
Subpotent Drug
Class II · Moderate risk
Rapidol Maximum Strength
CGMP Deviations
Other recalls by Island Kinetics, Inc. d.b.a. CoValence Laboratories
All 2026 recalls
Class II · Moderate risk
Blemish Spot Treatment
Failed Stability Specifications
Class III · Low risk
Essential Calming Skin Gel
Subpotent Drug
Class III · Low risk
Skin Rehab
Subpotent Drug
Class III · Low risk
PCA Skin Blemish Control Bar
Superpotent Drug: Salicylic acid content is above the firm's specification.
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