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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Low RiskFDA Drug
Medications & Supplements/Topical Products

Advantice Health: Dermoplast Pain & Itch Spray Recalled for Incorrect Net Weight Labeling

Agency Publication Date: April 30, 2019
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Summary

Advantice Health is recalling approximately 222,984 canisters of Dermoplast Anesthetic Pain & Itch (benzocaine and menthol) Spray because the packaging incorrectly states the net weight. The canisters are labeled as containing 2.75 oz (78g) of product, but they actually contain only 2.0 oz. This recall affects both individual canisters and full cases of 12 units sold nationwide in the United States. While the product inside is safe for use, the labeling error means consumers are receiving less medication than advertised on the package.

Risk

The risk is low; however, the labeling error causes consumers to receive approximately 27% less product than stated on the canister, which may lead to unexpected depletion of the medication during use.

What You Should Do

  1. Identify if you have the affected product by checking for Dermoplast Anesthetic PAIN & ITCH (benzocaine and menthol) SPRAY canisters with the net weight labeled as 2.75 oz (78g).
  2. Check the canister or the case packaging for Lot Number 14049A with an expiration date of 12/21 (December 2021).
  3. Verify the UPC codes: 8 51409 00722 6 for individual canisters or Case UPC 1 03 16864 68002 7 for full cases of 12 units (Product Code 80-6802).
  4. Contact your healthcare provider or pharmacist for guidance regarding the use of this product and return any unused spray to the place of purchase for a refund.
  5. Contact the manufacturer, Advantice Health (formerly distributed by Moberg Pharma North America LLC), for further instructions regarding this labeling correction.
  6. For additional questions, contact the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) or visit www.fda.gov/safety/recalls.

Your Remedy Options

๐Ÿ’ฐFull Refund

Contact your healthcare provider or pharmacist for guidance. Return any unused product to the pharmacy for a refund

How to: Contact your healthcare provider or pharmacist for guidance. Return any unused product to the pharmacy for a refund

Affected Products

Product: Dermoplast Anesthetic PAIN & ITCH (benzocaine and menthol) SPRAY canisters (2.75 oz / 78g)
Model:
D-1279-2019
UPC Codes:
851409007226
Lot Numbers:
14049A (Exp 12/21)
Date Ranges: Expiration 12/21
Product: Dermoplast Anesthetic PAIN & ITCH (benzocaine and menthol) SPRAY full case of 12-2 oz. cans
Model:
D-1280-2019
Product Code 80-6802
UPC Codes:
10316864680027
Lot Numbers:
14049A (Exp 12/21)
Date Ranges: Expiration 12/21

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 82709
Status: Resolved
Manufacturer: Advantice Health
Manufactured In: United States
Units Affected: 2 products (111,492 canisters total)
Distributed To: Nationwide
Agency Last Updated: May 14, 2019

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.