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Lower risk Drug recall · FDA · Published August 27, 2025

DermaRite Lantiseptic Skin Protectant Recall: Contamination Risk

DermaRite recalls Lantiseptic skin protectant due to contamination at shared manufacturing facility. Products with NDC 61924-304-05 to 61924-304-12 may be affected. Stop using if expired by 08/2027.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #D-0170-2026DrugDermaRite ›
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Contact the company

Recalling firmDermaRite Industries, LLC7777 W Side Ave · North Bergen, NJ 07047-6436
✎ GovInfoNow plain-language explainer

DermaRite is recalling Lantiseptic skin protectant products that were manufactured at a facility with contamination issues. This recall affects specific sizes and lot numbers that expired by August 2027. Using these products could expose you to contaminants from the shared facility. Read more at govinfonow.com/recall/31828-dermarite-lantiseptic-skin-protectant-recall-contamination-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/31828-dermarite-lantiseptic-skin-protectant-recall-contamination-risk · Updated August 17, 2026 · FDA enforcement record: FDA #D-0170-2026

Cite this page

“DermaRite Lantiseptic Skin Protectant Recall: Contamination Risk.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/31828-dermarite-lantiseptic-skin-protectant-recall-contamination-risk. Based on FDA recall #D-0170-2026 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0170-2026%22&limit=1).

The FDA announced on August 27, 2025, that DermaRite Industries, LLC is recalling Lantiseptic Skin Protectant due to current good manufacturing practice deviations. The agency stated the products were manufactured at a facility where other lots were found to be contaminated.

How to tell if you have it

  • Brand: DermaRite
  • Product: Lantiseptic, Skin Protectant, Lanolin USP 30%
  • NDC 61924-304-05 (5g / 0.17 oz)
  • NDC 61924-304-14 (14.2g / 0.5 oz)
  • NDC 61924-304-04 (4oz)
  • NDC 61924-304-45 (4.5oz)
  • NDC 61924-304-12 (12oz)
  • Lots on or before expiry date 08/2027
  • Sold nationwide in the USA

The hazard

According to the FDA, the recall is due to CGMP deviations. The agency reported that the products were manufactured at the same facility where other products and lots were found to be contaminated.

Context

GovInfoNow's records show DermaRite Industries, LLC has one other recall on record since July 17, 2025. On July 17, 2025, the company recalled PeriGiene Antiseptic due to microbial contamination with Burkholderia cepacia. Other recent recalls of similar products include Blaine Labs Revitaderm Gel Recall (April 8, 2026), Trifluent Pharma Wound Care Gel Recall (April 8, 2026), and Medline Silicone Cream Recall (June 11, 2026).

How to tell if you have this one

Check the product label for the NDC numbers 61924-304-05, 61924-304-14, 61924-304-04, 61924-304-45, or 61924-304-12. Products with expiration dates on or before August 2027 are included in this recall.

  • Brand
    DermaRite
  • Category
    Drug
FDA recall event · 18 products

All 18 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
    Ongoing
  • Distribution
    Nationwide in the USA
Recall numberProduct, codes & lotsQuantityNDC
D-0160-20264-N-1 Skin Protectant, No Rinse Wash Cream with Dimethicone 1%, 113g, (4 oz) per bottle, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-208-04; All lots on or before expiry date 08/2027.3,178 bottles—
D-0161-2026DermaCerin, Skin Protectant Moisturizing Cream (petrolatum 33%), packaged in a) 106 g (3.75 oz.) per tube (NDC 61924-174-04) and b) 454 g (16 oz.) per jar (NDC 61924-174-16), DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047.; All lots on or before expiry date 08/2027——
D-0162-2026DermaFungal, Antifungal Cream with 2% Miconazole Nitrate, packaged in a) 5 g (0.18 oz) per packet (NDC 61924-234-05), and b)106 g (3.75 oz.) per tube (NDC 61924-234-04) DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047.; All lots on or before expiry date 08/20271,480 packets—
D-0163-2026DermaKleen, Health Care Antiseptic Lotion Soap with Vitamin E, Chloroxylenol 0.2%, packaged in a) 222 mL (7.5 fl. oz.) per tube (NDC 61924-092-08), b) 800 mL (27 fl. oz.) per bag (NDC 61924-092-27), and c 1000 mL (34 fl. oz.) per bag (NDC 61924-092-34), DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047.; All lots on or before expiry date 08/20277,736 tubes—
D-0164-2026DermaMed Ointment, Skin Protectant, Aluminum Hydroxide Gel 2%, Net Wt. 106 g (3.75 oz.) per tube, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-214-04; All lots on or before expiry date 08/20272,673 tubes—
D-0165-2026DermaSarra, Camphor 0.5%, External Analgesic, 222 mL (7.5 fl. oz.) per bottle, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-189-08; All lots on or before expiry date 08/20272,389 bottles—
D-0166-2026GelRite Instant Hand Sanitizer, Alcohol 65%, packaged in a) 118 mL (NDC 61924-106-04), b) 473 mL (NDC 61924-106-16) and c) 800 mL (NDC 61924-106-27), and d) 1000 mL (NDC 61924-106-34) per container, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047.; All lots on or before expiry date 08/2027115,994 containers—
D-0167-2026Hand-E-Foam, Benzethonium Chloride 0.20%, packaged in a) 236mL (NDC 61924-102-08) and b) 1000 mL (NDC 61924-102-34) per container, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047.; All lots on or before expiry date 08/2027576 containers—
D-0168-2026KleenFoam Antimicrobial Foam Soap, Chloroxylenol 0.5%, 34 FL OZ (1000 mL) per cartridge, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-093-34; All lots on or before expiry date 08/202715,267 cartridges—
D-0169-2026Lantiseptic, Dry Skin Therapy, Lanolin USP 30%, packaged in a) 5 g (0.17 oz) (NDC 61924-504-05), b) 4 oz (NDC 61924-504-04), and c)14 oz (NDC 61924-710-14) tubes, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047.; All lots on or before expiry date 08/20278,378 containers—
D-0170-2026Lantiseptic, Skin Protectant, Lanolin USP 30%, packaged in a) 5g (0.17 oz) (NDC 61924-304-05), b)14.2g (0.5 oz)( NDC 61924-304-14), c) 4oz (NDC 61924-304-04), d) 4.5oz (NDC 61924-304-45), and e) 12oz (NDC 61924-304-12) tubes, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047.; All lots on or before expiry date 08/202757,837 units—
D-0171-2026McKesson Skin Protectant, Lanolin USP, packaged in a) 5g (NDC 68599-6202-1), and b) 4oz NDC 68599-6203-4 tube, Distributed by McKesson Medical-Surgical Inc., Richmond, VA 23233.; All lots on or before expiry date 08/20275,876 units68599-6202-1, 68599-6202-2, 68599-6202-4, 68599-6203-1, 68599-6203-4
D-0172-2026PeriGiene, Health Care Antiseptic, Chloroxylenol 0.5%, 222mL (7.5 fl. oz.) bottle, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-198-08; All lots on or before expiry date 08/202716,006 units—
D-0173-2026PeriGuard Ointment, Petrolatum 49.9%, packaged in a) 5g (NDC 61924-205-05), b) 3.5oz (NDC 61924-205-04), and c) 7oz (NDC 61924-205-07) tubes, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047.; All lots on or before expiry date 08/2027381,619 units—
D-0174-2026Renew PeriProtect, Zinc Oxide 12%, Dimethicone 1%, 113g (4 oz.) per tube, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-435-04; All lots on or before expiry date 08/202737,272 tubes—
D-0175-2026Renew Skin Repair Cream, Dimethicone 1.5%, packaged in a) 5g tube (NDC 61924-405-05), b) 4 oz tube (NDC 61924-405-04), and c) 800 mL (NDC 61924-405-27), DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047.; All lots on or before expiry date 08/202757,041 units—
D-0176-2026San-E-Foam, Alcohol 67%, 1000 mL (34 fl. oz.) per cartridge, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-107-34; All lots on or before expiry date 08/202715,465 cartridges—
D-0177-2026UltraSure Anti-Perspirant & Deodorant, Aluminum Sesquichlorohydrate 15%, 118 mL (4 fl. oz.), DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-266-04; All lots on or before expiry date 08/202737,379 spray bottles—
Based on the official FDA remedy

What to do — step by step

  1. Check Product Expiry

    Verify if your Lantiseptic product expires by August 2027 using the NDC numbers listed.

Where it went and when

Where it was distributed

Distributed nationwide.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

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 published this recall 3 months after the firm started it.

1. Firm started the recall: Aug 27, 202512. FDA classified it Class II: Nov 20, 202523. Published in FDA’s Enforcement Report: Nov 26, 202532025
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

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Keep exploring

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-0170-2026 (August 27, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0170-2026 to see it in context.
  • Plain-language summary written by qwen3:4b on August 17, 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.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA