FDA recall, , Moderate risk
Dabur Antifungal, Antibiotic and Hydrocortisone Creams and Ointments
Dabur Antifungal, Antibiotic and Hydrocortisone Creams and Ointments have CGMP deviations.
Summary by Recall Canary from the FDA notice
What happened
Dabur India Limited, of Dadra And Nagar Haveli, India, recalled multiple Med Pride, Lucky Super Soft, Rapidol, Lil Drug Store, Circle K, and Cura Hongos antifungal, antibiotic, and hydrocortisone creams and ointments due to CGMP deviations, deficiencies observed during FDA inspection. The products were distributed nationwide in the US.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medicine recalls:
- Check the FDA or company notice for instructions specific to this product.
- Ask your pharmacist or doctor whether your lot is affected and what to do.
Is yours affected?
Match the lot code and UPC listed under your product.
Incomplete list: 130 of 143 lot codes shown.
A UPC is the number printed under a barcode.
Med Pride, Hydrocortisone Cream 1%, Net Wt. 1 oz (28.3g) tubes
- UPC
- 3 52410 30503 0
- Lot code
- 001
- 002
- 013
- 016
- 031
- 032
- 033
- 045
- 046
- 047
Lucky Super Soft, First Aid Triple Antibiotic Ointment, Bacitracin zinc 400 units, neomycin sulphate
- Strength
- 3.5 mg
- UPC
- 8 08829 10372 4
- Lot code
- 0002
- 0003
Rapidol, Triple Antibiotic First Aid Ointment, Bacitracin Zinc 400 units, Neomycin Sulfate
- Strength
- 3.5 mg
- UPC
- 8 10096 77162 9
- Lot code
- 0004
Med Pride, Triple Antibiotic Ointment, Bacitracin Zinc (equivalent to 400 units), Neomycin Sulfate
- Strength
- 5 mg
- UPC
- 1 03 52410 30253 1
- Lot code
- 011
- 014
- 015
- 016
- 017
- 018
- 019
- 020
- 021
- 022
- 026
Med Pride, Hydrocortisone Cream 1%, Net Wt. 16oz (454g) tubes
- UPC
- 3 52410 305061
- Lot code
- 003
- 004
- 005
- 006
- 007
- 008
- 009
- 010
- 011
- 012
- 014
- 015
- 017
- 018
- 019
- 020
- 021
- 022
- 023
- 024
- 025
- 026
- 027
- 028
- 029
- 030
- 034
- 035
- 036
- 037
- 038
- 039
- 041
- 042
- 043
- 044
- 048
- 049
- 050
- 051
Lucky Super Soft, Antifungal Athlete's Foot Cream, Clotrimazole 1% Cream, Net Wt. 1.5 oz (42.5g) Tubes
- UPC
- 8 08829 10461 5
- Lot code
- 0001
- 0002
Med Pride, Bacitracin Zinc Ointment, 1oz (28.3g) per tube, 72 tubes per case, Manufactured for: Shield Line LLC, 59 Hook Road, Bayonne, NJ 07002 USA, Made in India, UPC X004WB4LKT.
- Lot code
- 022
- 023
- 024
Med Pride, Bacitracin Zinc Ointment, 500 units, 1oz (28.3g) tubes
- UPC
- 3 52410 30354 8
- Lot code
- 001
- 002
- 003
- 004
- 005
- 006
- 010
- 011
- 012
- 013
- 014
- 016
- 017
- 018
- 019
- 020
Lil Drug Store, Triple Antibiotic Ointment, Bacitracin Zinc (400 units), Neomycin Sulfate (
- Strength
- 3.5 mg
- UPC
- 3 66715 97310 8
- Lot code
- 0005
Med Pride, 1% Clotrimazole Antifungal Cream, Net Wt. 1oz (28.3g)
- UPC
- 3 524103 0244 2
- Lot code
- 001
- 002
- 003
- 004
- 005
- 006
- 007
- 008
- 009
- 010
- 011
- 012
- 013
Med Pride, Triple Antibiotic Ointment, Bacitracin Zinc 400 units, Neomycin Sulfate
- Strength
- 5 mg
- UPC
- 3 52410 30255 8
- Lot code
- 001
- 002
- 003
- 004
- 005
- 006
- 007
- 008
- 009
- 010
- 012
- 013
- 023
- 024
- 025
- 027
- 028
- 029
- 031
- 032
- 033
- 034
- 035
Cura Hongos, Crema Antifungica, Clotrimazole 1%, 2oz (57g) tubes, Dist by/por: Pharmadel LLC, New Castle, DE 19720
- UPC
- 8 52924 00683 1
- Lot code
- 0003
Circle K, triple antibiotic ointment, Bacitracin Zinc (400 units), Neomycin Sulfate (
- Strength
- 3.5 mg
- UPC
- 1 94283 65181 0
- Lot code
- 0001
- 0005
Med Pride, Bacitracin Zinc Ointment, 500 units, 0.9g packets Net Wt 130g, 144 count box
- UPC
- 3 52410 30352 4
- Lot code
- 007
- 008
- 009
- 015
- 016
Recall details
- Company began the recall
- Sold in
US Nationwide.
- Company
- Dabur India LimitedDadra And Nagar Haveli, India
- Hazard
- Manufacturing problem
- Risk
Moderate risk
Taking it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 99137
- Recall numbers
- D-0629-2026 to D-0642-2026
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report
Listed on Recall Canary
In FDA's weekly enforcement report
Classified by FDA
Summary updated
