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RECALL RECORD — CLASS IIRecall closedD0030-2015/FDA enforcement
New Gpc INC.·Cosmetics·Aug 7, 2014

Alcosulph Astringent Lotion, NET Contents: 1) 60 ML and 2) 120 ML

What you need to know

Class II

  • What happened

    Does Not Meet Monograph: NEW GPC INC. has recalled multiple Over-the-Counter Drug Products due to lack of drug listing, lack of OTC drug labeling requirements and labeled Not…

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. A safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

  • Action required

    Stop applying or using the product. Check the UPC and lot codes below, then return it to the retailer or contact the manufacturer about a refund or replacement.

Recall closed · classified by the FDADistribution not listedMore cosmetics

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Match before you discard

Product identification

Source: FDA COSMETICS

Brand nameNew Gpc INC.
Recalling firmNew Gpc INC.East Bank Demerara, Guyana
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • Batch Numbers: 304159, 211463, 308345
Distribution area

New York

United States

Quantity affected900 units
Recall initiationFDA report date: October 29, 2014
FDA recall numberD0030-2015

Beyond the headline

The recall, in context

New Gpc INC. initiated this cosmetics recall on August 7, 2014. The FDA enforcement report states: Does Not Meet Monograph: NEW GPC INC. has recalled multiple Over-the-Counter Drug Products due to lack of drug listing, lack of OTC drug labeling requirements and labeled Not Approved for sale in U.S.A.. The FDA report lists distribution as: New York.

The FDA enforcement report describes the reason as: Does Not Meet Monograph: NEW GPC INC. has recalled multiple Over-the-Counter Drug Products due to lack of drug listing, lack of OTC drug labeling requirements and labeled Not Approved for sale in U.S.A..

Alcosulph Astringent Lotion, NET Contents: 1) 60 ML and 2) 120 ML was made or distributed by New Gpc INC. in East Bank Demerara, Guyana. This page reflects FDA report D0030-2015, dated October 29, 2014.

Why this is a Class II recall

Class II means the product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. In this recall, a safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

FDA definition

The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote.

What to do now

  1. 1

    Stop using it

    Set the product aside and do not apply it.

  2. 2

    Check the codes

    Compare the lot and date codes against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Product safety recall

Symptoms to watch for

The official enforcement report describes the specific risk. Follow the recall notice, check the product codes and do not use a product that may be affected.

Higher-risk groups

Children, pregnant people, older adults and people with weakened immune systems should take extra care when a product's safety is uncertain.

What to do now

  1. 1Stop using or eating the product and keep it away from children and pets.
  2. 2Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return.
  3. 3Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Read the official source record for the specific hazard and instructions.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Alcosulph Astringent Lotion, NET Contents: 1) 60 ML and 2) 120 ML recall?

New Gpc INC. recalled Alcosulph Astringent Lotion, NET Contents: 1) 60 ML and 2) 120 ML in an FDA Class II enforcement action reported as D0030-2015. Does Not Meet Monograph: NEW GPC INC. has recalled multiple Over-the-Counter Drug Products due to lack of drug listing, lack of OTC drug labeling requirements and labeled Not…

What should I do if I bought this product?

Stop applying or using the product. Check the UPC and lot codes below, then return it to the retailer or contact the manufacturer about a refund or replacement. Stop using or eating the product and keep it away from children and pets. Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return. Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Is the New Gpc INC. recall still active?

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record D0030-2015. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

Brand history

More recalls by New Gpc INC.

View brand
Class II·

New Gpc INC.

Whitfield Lotion, NET Contents: 60 ML

Does Not Meet Monograph: NEW GPC INC. has recalled multiple Over-the-Counter Drug Products due to lack of drug listing, lack of OTC drug labeling requirements and labeled Not…

Distribution not listedCosmetics

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.