Lucky Mart recalls PIYANPING Anti-Itch Lotion with dexamethasone instead of hydrocortisone
Lucky Mart recalls PIYANPING Anti-Itch Lotion (1% hydrocortisone) due to incorrect formulation containing dexamethasone. This may cause adverse reactions. Check NDC 68085-8012-4 and lots C16001/C16002.
Lower-risk recall
Incorrect Product Formulation: product contains dexamethasone instead of hydrocortisone.
Contact the company
What happened, in plain English
Lucky Mart is recalling PIYANPING Anti-Itch Lotion because it contains dexamethasone instead of hydrocortisone. Using this lotion could cause adverse reactions like skin irritation or allergic responses. This is a safety issue for people using the product for itching relief. Read more at govinfonow.com/recall/41294-lucky-mart-recalls-piyanping-anti-itch-lotion-with-dexamethasone-instead.
Source Summary by GovInfoNow · govinfonow.com/recall/41294-lucky-mart-recalls-piyanping-anti-itch-lotion-with-dexamethasone-instead · Updated October 7, 2026 · FDA enforcement record: FDA #D-0031-2018
Cite this page
“Lucky Mart recalls PIYANPING Anti-Itch Lotion with dexamethasone instead of hydrocortisone.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/41294-lucky-mart-recalls-piyanping-anti-itch-lotion-with-dexamethasone-instead. Based on FDA recall #D-0031-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0031-2018%22&limit=1).
Why it’s dangerous
The product was formulated with dexamethasone instead of hydrocortisone. Dexamethasone is a stronger corticosteroid that can cause more severe skin reactions compared to hydrocortisone.
Who’s affected
People who own or use the recalled PIYANPING Anti-Itch Lotion (1% hydrocortisone) tube. Those with sensitive skin or allergies may be at higher risk of reactions.
How to tell if you have this one
Check for the product name 'PIYANPING Anti-Itch Lotion', 1% concentration, 0.67 oz (20g) tube, manufactured by Jimin Pharmaceutial Co., LTD. and distributed by Lucky Mart. Look for NDC 68085-8012-4 and lots C16001 or C16002.
- Brand
Lucky Mart- Category
Drug
What to do — step by step
Check Product Details
Verify the product name, concentration, and lot numbers to confirm if it's recalled.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “Nationwide in the USA” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 14 months after the firm started it.
- Firm started the recall
- FDA classified it Class I
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #D-0031-2018 (August 29, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0031-2018 to see it in context.
- Plain-language summary written by qwen3:4b on October 7, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.