Teligent Pharma Triamcinolone Ointment Recall: Mispackaged Product
Teligent Pharma recalls 0.1% Triamcinolone Acetonide Ointment USP 80g cartons due to incorrect labeling. This Rx-only product may be mispackaged and should be checked for proper labeling.
Lower-risk recall
Correct Labeled Product Mispack
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What happened, in plain English
Teligent Pharma is recalling 0.1% Triamcinolone Acetonide Ointment USP 80g cartons because they were mispackaged. This recall affects prescription-only products that may have incorrect labeling, which could lead to improper use. Read more at govinfonow.com/recall/36069-teligent-pharma-triamcinolone-ointment-recall-mispackaged-product.
Source Summary by GovInfoNow · govinfonow.com/recall/36069-teligent-pharma-triamcinolone-ointment-recall-mispackaged-product · Updated August 18, 2026 · FDA enforcement record: FDA #D-0752-2021
Cite this page
“Teligent Pharma Triamcinolone Ointment Recall: Mispackaged Product.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/36069-teligent-pharma-triamcinolone-ointment-recall-mispackaged-product. Based on FDA recall #D-0752-2021 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0752-2021%22&limit=1).
Why it’s dangerous
The product was mispackaged, meaning the labeling might not match the actual contents. This could lead to incorrect usage if the patient uses the wrong medication. However, the recall is for labeling issues, not safety risks.
Who’s affected
Prescription patients who have received this specific ointment product. Those with medical conditions requiring this medication are most at risk if mislabeled.
How to tell if you have this one
Check for the product name 'Triamcinolone Acetonide Ointment USP 0.1% 80g', manufacturer 'Teligent Pharma', and lot number 16630 with expiration 03/2023.
- Brand
Teligent Pharma- Category
Drug
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class II- Status
Terminated- Distribution
Nationwide
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| D-0751-2021 | Econazole Nitrate Cream 1%, 85 grams bulk shippers, Rx Only, Teligent Pharma, Inc. Buena, New Jersey 08310, NDC 52565-022-85 ; packaged in tubes.; Lot # 16630; Exp 03/2023 | 14688 tubes |
| D-0752-2021 | Triamcinolone Acetonide Ointment USP, 0.1% 80 g cartons, Rx Only, Teligent Pharma, Inc. Buena, New Jersey 08310, NDC 52565-014-80 ; packaged in tubes.; Lot # 16630; Exp 03/2023 | N/A |
What to do — step by step
Check Labeling
Verify the product label matches the correct information: Triamcinolone Acetonide Ointment USP 0.1% 80g, Teligent Pharma, Lot #16630, Exp 03/2023.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “Nationwide” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 3.1 years after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
Questions people ask
Is this product safe to use?
The recall is for mispackaging, not safety risks. The product is safe if labeled correctly, but you should check the label to ensure it matches the specified details.
Do I need to stop using this product?
No, but you should check the label to ensure it matches the correct details before using. If it doesn't match, contact your healthcare provider.
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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-0752-2021 (July 19, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0752-2021 to see it in context.
- Plain-language summary written by qwen3:4b on August 18, 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.