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Unrated Drug recall · FDA · Published November 25, 2019

OraLabs Petroleum Jelly Recall: Cross Contamination Risk

OraLabs recalls petroleum jelly tubes with undeclared phenol and camphor. Consumers should check UPCs 1182298884 and 1182298541 for affected products.

🇺🇸 FDA recall #D-0624-2020DrugOraLabs ›
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Recalling firmOraLabs, Incorporated18685 Plaza Dr · Parker, CO 80134-9061
✎ GovInfoNow plain-language explainer

OraLabs is recalling petroleum jelly tubes that may contain undeclared phenol and camphor. This cross-contamination could cause health issues if used. Read more at govinfonow.com/recall/37672-oralabs-petroleum-jelly-recall-cross-contamination-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/37672-oralabs-petroleum-jelly-recall-cross-contamination-risk · Updated October 5, 2026 · FDA enforcement record: FDA #D-0624-2020

Cite this page

“OraLabs Petroleum Jelly Recall: Cross Contamination Risk.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/37672-oralabs-petroleum-jelly-recall-cross-contamination-risk. Based on FDA recall #D-0624-2020 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0624-2020%22&limit=1).

The FDA announced on Nov. 25, 2019, that OraLabs, Incorporated voluntarily recalled petroleum jelly products due to cross-contamination with undeclared phenol and camphor. Owners should contact the company for a refund. GovInfoNow's records show this Class II recall was initiated by the firm.

How to tell if you have it

  • OraLabs Petroleum jelly (White Petrolatum) USP 100%
  • 1 oz tube, UPC 1182298884
  • 2.5 oz tube, UPC 1182298541
  • Lot #44660922, Exp. 09/22
  • Lot #44771122, Exp. 11/22

The hazard

The petroleum jelly tubes contained undeclared contaminants of phenol and camphor due to cross-contamination with other products. The FDA classified this as a Class II recall.

Context

GovInfoNow's records show OraLabs has been involved in previous recalls, including the Dec. 26, 2025, petroleum jelly contamination recall by Gold Star Distribution. Other recent recalls of similar products include the Keystone Dental City Topical Anesthetic Gel Recall (May 21, 2026) and the Broadway Joe's Pain Cream Recall (Aug. 21, 2026).

How to tell if you have this one

Check for UPCs 1182298884 (1 oz tube) or 1182298541 (2.5 oz tube). The products were distributed by Rite Aid with specific expiration dates.

  • Brand
    OraLabs
  • Product
    Petroleum jelly (White Petrolatum) USP 100%, packaged in a) 1 oz tube (UPC 1182298884), b) 2.5 oz tube (UPC
  • Category
    Drug
Based on the official FDA remedy

What to do — step by step

  1. Check Product UPC

    Look for the UPC numbers 1182298884 or 1182298541 on the tube packaging.

Where it went and when

Where it was distributed

Distributed nationwide.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “Nationwide within the United States” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA terminated this recall 14 months after the firm started it.

1. Firm started the recall: Nov 25, 201912. Published in FDA’s Enforcement Report: Dec 18, 201923. FDA classified it Class II: Dec 19, 201934. FDA terminated the recall: Jan 27, 2021420192021
  1. Firm started the recall
  2. Published in FDA’s Enforcement Report
  3. FDA classified it Class II
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #D-0624-2020 (November 25, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0624-2020 to see it in context.
  • Plain-language summary written by qwen3:4b on October 5, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA