glo Skin Beauty Remedy Gel recalled as a subpotent hydrocortisone product
Remedy Gel, hydrocortisone 1%, distributed by glo Skin Beauty is being recalled because the product is subpotent. The action covers 1,060 bottles.
The agency’s classification
FDA (Drugs): Class III
Class III is a situation in which use of or exposure to a violative product is not likely to cause adverse health consequences.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 2/5 (Moderate).
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: FDA Class III recall for subpotency, which the rubric places in the 1-2 band; a potency shortfall rather than a purely cosmetic issue puts it at Moderate.
Plain-English summary
Remedy Gel, hydrocortisone 1%, in 30 mL (1 fl oz) bottles, NDC 66915-531-12 and 66915-531-13, is being recalled. The product is distributed by glo Skin Beauty of Denver, Colorado. The action covers 1,060 bottles.
The stated reason is that the drug is subpotent, meaning it contains less active ingredient than the label declares. The FDA classified the action as Class III, its least serious classification, which is applied where use of the product is not likely to cause adverse health consequences.
Affected lots are 4155D2 and 4155D3, expiry 05/15/2026. Distribution was US nationwide.
Consumers who have an affected lot should stop using it and contact the retailer or the firm about a refund or replacement.
The recalled product
- Product
- 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
- Category
- Drug — Topical corticosteroid
- Affected units
- 1,060
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (3)
- Lot 4155D2
- 4155D3
- Exp. 05/15/2026
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 3 recalled by Island Kinetics, Inc. d.b.a. CoValence Laboratories under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 3 products in this recall →Related recalls
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