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Lower risk Drug recall · FDA · Published May 4, 2018

Milbar T Shampoo Recall: Subpotent Coal Tar Risk

Milbar recalls coal tar shampoo bottles with subpotent coal tar content. This may not deliver intended treatment for skin conditions. Consumers should check lot numbers and expiration dates.

🇺🇸 FDA recall #D-0832-2018DrugMilbar ›
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Recalling firmMilbar Laboratories, Inc.20 Commerce St · East Haven, CT 06512-4145
✎ GovInfoNow plain-language explainer

What happened, in plain English

Milbar is recalling shampoo bottles that contain coal tar for skin conditions. The product may not have enough active ingredient to treat skin issues as intended, which could lead to ineffective treatment. Read more at govinfonow.com/recall/40570-milbar-t-shampoo-recall-subpotent-coal-tar-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/40570-milbar-t-shampoo-recall-subpotent-coal-tar-risk · Updated October 7, 2026 · FDA enforcement record: FDA #D-0832-2018

Cite this page

“Milbar T Shampoo Recall: Subpotent Coal Tar Risk.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/40570-milbar-t-shampoo-recall-subpotent-coal-tar-risk. Based on FDA recall #D-0832-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0832-2018%22&limit=1).

Why it’s dangerous

The shampoo has subpotent coal tar, meaning it contains less active ingredient than intended. This could result in the product not working well for skin conditions. It does not pose a direct physical danger like burns or injury.

Who’s affected

People who use this shampoo for skin conditions like psoriasis or eczema. Those with sensitive skin may be at higher risk of ineffective treatment.

How to tell if you have this one

Check for lot numbers MT390-8 (expiring 12/01/2020) or GU925-4 (expiring 07/05/2020) on the bottle. The product is a 300 ml/10.1 fl. oz. bottle labeled as a dermatological cosmetic.

  • Brand
    Milbar
  • Category
    Drug
FDA recall event · 2 products

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 III
  • Status
    Terminated
  • Distribution
    Product was distributed to physicians and internet sales throughout the United States and Hong Kong, Panama, UK, China, Jordan, Qatar, Kuwait, and Central America.
Recall numberProduct, codes & lotsQuantity
D-0832-2018T Shampoo For Hair and Body, Solution Coal Tar 3% (0.6% coal tar), 300 ml/10.1 fl. oz. bottles, Dermatologic Cosmetic Laboratories, East Haven, CT; Lot # MT390-8, expiration date 12/01/2020 GU925-4, expiration date 07/05/2020952 bottles
D-0833-2018Zoma Shampoo, Zinc Pyrithione 1.92%, 300 ml/10.01 fl. oz. bottles, Dermatologic Cosmetic Laboratories, East Haven, CT; Lot # HT659-6, expiration date 08/11/2019 LT168-7, expiration date 11/10/20191,348 bottles
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Look for lot numbers MT390-8 (expiring 12/01/2020) or GU925-4 (expiring 07/05/2020) on the bottle.

Where it went and when

Where it was distributed

Distributed nationwide, and outside the U.S.

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: “Product was distributed to physicians and internet sales throughout the United States and Hong Kong, Panama, UK, China, Jordan, Qatar, Kuwait, and Central America.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide, and outside the U.S.

Recall timeline

FDA terminated this recall 10 months after the firm started it.

1. Firm started the recall: May 4, 201812. FDA classified it Class III: May 22, 201823. Published in FDA’s Enforcement Report: May 30, 201834. FDA terminated the recall: Mar 18, 2019420182019
  1. Firm started the recall
  2. FDA classified it Class III
  3. Published in FDA’s Enforcement Report
  4. 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-0832-2018 (May 4, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0832-2018 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.
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