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Class II: temporary or reversible health riskCompleted

Ecometics Unguentine Ointment Recall

Unguentine Ointment, (Camphor 3

Ecometics, Inc. · Norwalk, CT

Risk level
Class II
Reported by FDA
Aug 30, 2023
Recall ID
D-1099-2023
Check your lot numberHow we source this data

Summary

Ecometics recalled Unguentine Ointment starting Aug 9, 2023. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-1099-2023 on Aug 30, 2023. Reason: CGMP Deviations: Products not manufactured under current good manufacturing practices. Status: Completed.

Why it was recalled

CGMP Deviations: Products not manufactured under current good manufacturing practices.

Product description

Unguentine Ointment, (Camphor 3.0%, Phenol 2.5%, Tannic Acid 2.2%, Zinc Oxide 6.6%), labeled as a) NET WT 1 OZ (28 g) tubes, Improved Formula, UPC 0 11169 10216 0, and b) NET WT 1 OZ (28.3g) tubes, Maximum Strength, UPC 0 11169 11250 3, Distributed by: Oakhurst Company, Levittown, NY 11756.

Lot numbers, UPCs & expiration codes

a) and b) 1E113A, exp 4/24

Where it was sold

Nationwide in the USA

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-1099-2023
Classification
Class II
Status
Completed
Recall initiated
Aug 9, 2023
FDA report date
Aug 30, 2023
Quantity
a) 6,120 tubes, b) 540 tubes
Recall type
Voluntary: Firm initiated
Recalling firm
Ecometics, Inc.

Original FDA data

Every field from FDA enforcement report D-1099-2023, exactly as published.

Show all FDA fields
City
Norwalk
State
CT
Status
Completed
Country
United States
Event ID
92857
Address
19 Concord St
Code information
a) and b) 1E113A, exp 4/24
Postal code
06854-3706
Report date
Aug 30, 2023
Product type
Drugs
Recall number
D-1099-2023
Classification
Class II
Recalling firm
Ecometics, Inc.
Product quantity
a) 6,120 tubes, b) 540 tubes
Reason for recall
CGMP Deviations: Products not manufactured under current good manufacturing practices.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Unguentine Ointment, (Camphor 3.0%, Phenol 2.5%, Tannic Acid 2.2%, Zinc Oxide 6.6%), labeled as a) NET WT 1 OZ (28 g) tubes, Improved Formula, UPC 0 11169 10216 0, and b) NET WT 1 OZ (28.3g) tubes, Maximum Strength, UPC 0 11169 11250 3, Distributed by: Oakhurst Company, Levittown, NY 11756.
Distribution pattern
Nationwide in the USA
Recall initiation date
Aug 9, 2023
Initial firm notification
Letter
Center classification date
Aug 24, 2023

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-1099-2023, published Aug 30, 2023. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

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