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Class II: temporary or reversible health riskTerminated

Victus Hipoglos Ointment Recall

Hipoglos Ointment (zinc oxide and lanolin), Helps prevent and treat diaper rash, skin i…

Victus, Inc. · Miami, FL

Risk level
Class II
Reported by FDA
Aug 29, 2012
Recall ID
D-1652-2012
Check your lot numberHow we source this data

Summary

Victus recalled Hipoglos Ointment starting Nov 10, 2011. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-1652-2012 on Aug 29, 2012. Reason: Misbranded. Status: Terminated.

Why it was recalled

Misbranded

Product description

Hipoglos Ointment (zinc oxide and lanolin), Helps prevent and treat diaper rash, skin irritation, Manufactured by Laboratorios Andromaco S.A. Av. Quilin 5273, Penalolen, Santiago. www.hipoglos.cl, www.laboratoriosandromaco.cl, Made in Chile, Net wt. per Tube: a) 0.18 oz (5 g), NDC: 50145-111-05; b) 2.2 oz (60 g), NDC: 50145-111-04; c) 2.5 oz (72 g), NDC: 50145-111-03; d) 3.5 oz (100 g), NDC: 50145-111-02; e) 4.2 oz (120 g), NDC: 50145-111-01.

Lot numbers, UPCs & expiration codes

Lot #/Product #: a) C1557B/MM26306, Exp 03/31/2014; b) C1387B/PV16856, Exp 03/31/2014, G0288C/PV16856, Exp 07/31/2013; c) G0288A/PV16855, Exp 07/31/2013; d) G0289B/PV16854, Exp 07/31/2013; e) C1387A/PV16853, Exp 03/31/2014, G0288B/PV16853, Exp 07/31/2013

Where it was sold

FL

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-1652-2012
Classification
Class II
Status
Terminated
Recall initiated
Nov 10, 2011
FDA report date
Aug 29, 2012
Quantity
1,535 Tubes
Recall type
Voluntary: Firm initiated
Recalling firm
Victus, Inc.

Original FDA data

Every field from FDA enforcement report D-1652-2012, exactly as published.

Show all FDA fields
City
Miami
State
FL
Status
Terminated
Country
United States
Event ID
62541
Address
4918 SW 74th Ct
Code information
Lot #/Product #: a) C1557B/MM26306, Exp 03/31/2014; b) C1387B/PV16856, Exp 03/31/2014, G0288C/PV16856, Exp 07/31/2013; c) G0288A/PV16855, Exp 07/31/2013; d) G0289B/PV16854, Exp 07/31/2013; e) C1387A/PV16853, Exp 03/31/2014, G0288B/PV16853, Exp 07/31/2013
Postal code
33155-4400
Report date
Aug 29, 2012
Product type
Drugs
Recall number
D-1652-2012
Classification
Class II
Recalling firm
Victus, Inc.
Product quantity
1,535 Tubes
Termination date
Jul 25, 2013
Reason for recall
Misbranded
Voluntary / mandated
Voluntary: Firm initiated
Product description
Hipoglos Ointment (zinc oxide and lanolin), Helps prevent and treat diaper rash, skin irritation, Manufactured by Laboratorios Andromaco S.A. Av. Quilin 5273, Penalolen, Santiago. www.hipoglos.cl, www.laboratoriosandromaco.cl, Made in Chile, Net wt. per Tube: a) 0.18 oz (5 g), NDC: 50145-111-05; b) 2.2 oz (60 g), NDC: 50145-111-04; c) 2.5 oz (72 g), NDC: 50145-111-03; d) 3.5 oz (100 g), NDC: 50145-111-02; e) 4.2 oz (120 g), NDC: 50145-111-01.
Distribution pattern
FL
Recall initiation date
Nov 10, 2011
Initial firm notification
Telephone
Center classification date
Aug 17, 2012

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-1652-2012, published Aug 29, 2012. 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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