Key facts
| Recalling firm | Dabur India Limited |
|---|---|
| Manufacturer | Not disclosed in the FDA record. |
| Brand name | Not disclosed in the FDA record. |
| Product description | Lucky Super Soft, Antifungal Athlete's Foot Cream, Clotrimazole 1% Cream, Net Wt. 1.5 oz (42.5g) Tubes, Manufactured for Delta Brands Inc., 580 White Plains Rd., Tarrytown, NY 10591 USA, Made in India, UPC 8 08829 10461 5. |
| Classification | Class II |
| Recall number | D-0629-2026 |
| Report date | Not disclosed in the FDA record. |
| Status | Ongoing |
| Reason for recall | CGMP Deviations; deficiencies observed during FDA inspection |
What consumers should do
Because this recall carries FDA's middle severity classification, anyone who has this product should stop using it and follow the recalling firm's instructions, even though serious harm is considered unlikely for this classification. Specifically, check whether the product in your possession matches the description on file with FDA -- Lucky Super Soft, Antifungal Athlete's Foot Cream, Clotrimazole 1% Cream, Net Wt. 1.5 oz (42.5g) Tubes, Manufactured for Delta Brands Inc., 580 White Plains Rd., Tarrytown, NY 10591 USA, Made in India, UPC 8 08829 10461 5. -- and the recall number D-0629-2026. If it matches, stop using or distributing it and contact Dabur India Limited or the point of purchase for return or replacement instructions. Retailers and distributors holding affected inventory should quarantine it and follow the firm's written recall notice.
What this classification means
FDA classifies a recall as Class II when using the recalled product, or being exposed to it, may cause temporary or medically reversible adverse health consequences, or when the probability of serious adverse health consequences is remote. In this case, the recalling firm is Dabur India Limited and the affected product is described in FDA's record as: Lucky Super Soft, Antifungal Athlete's Foot Cream, Clotrimazole 1% Cream, Net Wt. 1.5 oz (42.5g) Tubes, Manufactured for Delta Brands Inc., 580 White Plains Rd., Tarrytown, NY 10591 USA, Made in India, UPC 8 08829 10461 5.. FDA's stated reason for the recall is: CGMP Deviations; deficiencies observed during FDA inspection. The recall is tracked under FDA recall number D-0629-2026 and carries a status of Ongoing as of the most recent FDA enforcement report. This classification reflects FDA's assessment of the product defect described above, not a prediction about any specific patient outcome. FDA maintains a public enforcement report database so that consumers, physicians, and purchasers can look up the exact product identifiers involved before deciding what to do. Recall status can change while FDA and the recalling firm continue corrective actions, so checking the firm's own notice for the most current guidance is recommended.
Dabur India Limited’s FDA history
Argus HQ has recorded 15 total FDA actions tied to Dabur India Limited: 0 warning letters, 14 recalls, 0 approval records, and 1 Form 483 inspection citation.
Frequently asked questions
- Where can I verify this recall directly with FDA?
- The verbatim FDA record is the source of truth for every recall Argus HQ tracks — always confirm against fda.gov before acting.
- What was recalled and why?
- Dabur India Limited recalled Lucky Super Soft, Antifungal Athlete's Foot Cream, Clotrimazole 1% Cream, Net Wt. 1.5 oz (42.5g) Tubes, Manufactured for Delta Brands Inc., 580 White Plains Rd., Tarrytown, NY 10591 USA, Made in India, UPC 8 08829 10461 5.. FDA's record states the reason for recall as: CGMP Deviations; deficiencies observed during FDA inspection. The recall is logged under FDA recall number D-0629-2026 with a Class II classification.
- How serious is this recall?
- FDA classifies a recall as Class II when using the recalled product, or being exposed to it, may cause temporary or medically reversible adverse health consequences, or when the probability of serious adverse health consequences is remote.
- What should someone who has this product do?
- Because this recall carries FDA's middle severity classification, anyone who has this product should stop using it and follow the recalling firm's instructions, even though serious harm is considered unlikely for this classification. Check the product against FDA's description (Lucky Super Soft, Antifungal Athlete's Foot Cream, Clotrimazole 1% Cream, Net Wt. 1.5 oz (42.5g) Tubes, Manufactured for Delta Brands Inc., 580 White Plains Rd., Tarrytown, NY 10591 USA, Made in India, UPC 8 08829 10461 5.) and recall number D-0629-2026, then follow Dabur India.
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Related enforcement actions
Full FDA history for Dabur India LimitedCompiled by Argus HQ Research from FDA primary sources · Reviewed by Andy Gaber, Founder
Cite this record
Reusing this data in reporting or research? Here’s a ready-made citation.
Argus HQ Research (2026). Recall Record: Class II Recall: Lucky Super Soft, Antifungal Athlete's Foot Cream, Clotrimazole… by Dabur India Limited. Digital Empire LLC. Retrieved from https://argushq.ai/recall/fda-recall-dabur-india-limited-d-0629-2026
"Recall Record: Class II Recall: Lucky Super Soft, Antifungal Athlete's Foot Cream, Clotrimazole… by Dabur India Limited." Argus HQ Research, Digital Empire LLC, 2026, argushq.ai/recall/fda-recall-dabur-india-limited-d-0629-2026.
Argus HQ Research. "Recall Record: Class II Recall: Lucky Super Soft, Antifungal Athlete's Foot Cream, Clotrimazole… by Dabur India Limited." Digital Empire LLC. Accessed July 13, 2026. https://argushq.ai/recall/fda-recall-dabur-india-limited-d-0629-2026.
@misc{argushq_argushq_ai_recall_fda_recall_dabur_india_limited_d_0629_2026_2026,
title = {Recall Record: Class II Recall: Lucky Super Soft, Antifungal Athlete's Foot Cream, Clotrimazole… by Dabur India Limited},
author = {{Argus HQ Research}},
year = {2026},
publisher = {Digital Empire LLC},
url = {https://argushq.ai/recall/fda-recall-dabur-india-limited-d-0629-2026},
note = {Accessed: July 13, 2026}
}Source: FDA.gov — Recalls ↗

