PlainRecalls
LowClass IIITerminated

FDA Drug recall · Reported September 29, 2021

Hydroquinone, USP, 4% Skin Bleaching Cream, packaged in 1 oz (28.35g) tube, Rx only, Manufactured for: Westminster Pharmaceuticals, LLC Nashville, TN 37217, NDC 69367-174-01 UPC 3 69367 17401 5

Subpotency: one product for active ingredient assay and another one for preservative assay

Recall #
D-0818-2021
Affected scope
6305 tubes
Initiated
September 1, 2021
Compiled from official public sources by the editorial team.
Verify with FDA Drug →
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Monarch Pcm, LLC recalled Hydroquinone, USP, 4% Skin Bleaching Cream, packaged in 1 oz (28.35g) tube, Rx only, Man… - a low-severity action.

Hydroquinone, USP, 4% Skin Bleaching Cream, packaged in 1 oz (28.35g) tube, Rx only, Man… was recalled by Monarch Pcm, LLC in September 29, 2021. Reason: Subpotency: one product for active ingredient assay and another one for preservative assay. Check the official notice for the remedy. Verify recall #D-0818-2021 with the FDA Drug before acting.

The recall

Monarch Pcm, LLC issued this low-severity FDA Drug recall-Subpotency: one product for active ingredient assay and another one for preservative assay.

Low
severity level
Class III
classification
September 29, 2021
reported

Sourced from official FDA Drug enforcement records. Verify recall #D-0818-2021 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

Recall Insight

This FDA Drug action (record #D-0818-2021) was formally reported on September 29, 2021, with the manufacturer initiating the action on September 1, 2021. It is classified under Low severity (Class III), with a current status of Terminated. Monarch Pcm, LLC is listed as the recalling firm, operating out of Fort Worth, TX. Federal records list the affected scope as 6305 tubes.

The documented reason for this recall is: Subpotency: one product for active ingredient assay and another one for preservative assay Distribution data in the federal record shows the product reached: OH, TN. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.

Within the same product category the archive holds 6 closely related recalls, 3 from FDA Drug - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.

Cosmetics & Personal Care recalls over time

Where this recall sits in its category - 1,360 cosmetics & personal care recalls on record

-1000100200300400 20052008201120142017202020232026 22
Severity2487872426High severity (most serious)Moderate severityLow severity
Where this recall sits in the database

Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified low severity.

Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.

Severity

Low

Affected scope

6305 tubes

Related Recalls

6

3 from same agency

Product description

Hydroquinone, USP, 4% Skin Bleaching Cream, packaged in 1 oz (28.35g) tube, Rx only, Manufactured for: Westminster Pharmaceuticals, LLC Nashville, TN 37217, NDC 69367-174-01 UPC 3 69367 17401 5

Reason for recall

Subpotency: one product for active ingredient assay and another one for preservative assay

Recall Profile

Structured summary of the FDA Drug recall record
Attribute Value
Agency U.S. Food and Drug Administration
Severity class Low (Class III)
Status Terminated
Recall number D-0818-2021
Date reported September 29, 2021
Date initiated September 1, 2021
Recalling firm Monarch Pcm, LLC
Firm location Fort Worth, TX
Affected scope 6305 tubes
Distribution OH, TN

Profile values are sourced directly from the official FDA Drug enforcement record. Source: U.S. Food and Drug Administration.

What to do with this recall

Match your product against the recall record, then act on the agency remedy.

  • Check the recall number (D-0818-2021) and product description against the item you own. Search the archive
  • Confirm the current status with FDA Drug before acting, recall details can be updated.
  • Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next

This page summarizes the official FDA Drug record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.

Frequently Asked Questions

What product was recalled?
Hydroquinone, USP, 4% Skin Bleaching Cream, packaged in 1 oz (28.35g) tube, Rx only, Manufactured for: Westminster Pharmaceuticals, LLC Nashville, TN 37217, NDC 69367-174-01 UPC 3 69367 17401 5. Recalled by Monarch Pcm, LLC. Units affected: 6305 tubes.
Why was this product recalled?
Subpotency: one product for active ingredient assay and another one for preservative assay
Which agency issued this recall?
This recall was issued by the FDA Drug on September 29, 2021. Severity: Low. Recall number: D-0818-2021.
Where was the recalled product distributed?
Distribution: OH, TN.
How do I check if my product is affected by a recall?
Check the product description and recall number (D-0818-2021) against your product. Visit the official FDA Drug website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device?
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.

Nearby Recalls in This Category

Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.

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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Drug, reported September 29, 2021. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.