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Stop using now Drug recall · FDA · Published June 3, 2020

Rocky Mountain Sunscreen SPF30 Lip Balm Recall: High Octisalate Content Risk

Rocky Mountain Sunscreen recalls SPF30 Kiwi Flavored Lip Balm due to excessive Octisalate (15% above label). Consumers should check product details and contact the manufacturer for guidance.

🇺🇸 FDA recall #D-1540-2020DrugRocky Mountain Sunscreen ›
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Contact the company

Recalling firmYusef Manufacturing Laboratories, LLCFreeport West, F-4, #3 · Clearfield, UT 84016
✎ GovInfoNow plain-language explainer

What happened, in plain English

Rocky Mountain Sunscreen is recalling its SPF30 Kiwi Flavored Lip Balm because it contains 15% more Octisalate than labeled. This high concentration of a chemical linked to potential health risks means users should stop using the product immediately. Read more at govinfonow.com/recall/37071-rocky-mountain-sunscreen-spf30-lip-balm-recall-high-octisalate-content.

Source Summary by GovInfoNow · govinfonow.com/recall/37071-rocky-mountain-sunscreen-spf30-lip-balm-recall-high-octisalate-content · Updated October 5, 2026 · FDA enforcement record: FDA #D-1540-2020

Cite this page

“Rocky Mountain Sunscreen SPF30 Lip Balm Recall: High Octisalate Content Risk.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/37071-rocky-mountain-sunscreen-spf30-lip-balm-recall-high-octisalate-content. Based on FDA recall #D-1540-2020 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1540-2020%22&limit=1).

Why it’s dangerous

The lip balm contains Octisalate at 15% above the labeled amount. This higher concentration of a chemical known to be a potential health risk in excessive amounts could cause adverse reactions, especially in sensitive skin or with prolonged use.

Who’s affected

Anyone who owns or uses the Rocky Mountain Sunscreen SPF30 Kiwi Flavored Lip Balm (0.15 oz tube) is affected. People with sensitive skin or those using the product frequently may be at higher risk due to the chemical concentration.

How to tell if you have this one

Check for the 0.15 oz tube labeled 'Rocky Mountain Sunscreen SPF30 Kiwi Flavored Lip Balm' with UPC 7 54018 20004 3 or Part ID 9PRKY01. The batch number starts with 13852.

  • Brand
    Rocky Mountain Sunscreen
  • Product
    Rocky Mountain Sunscreen SPF30 Kiwi Flavored Lip Balm (Oxybenzone 5%, Meradimate 5%, Octinoxate 7.5%, Octisalate 5%)
  • Category
    Drug
Based on the official FDA remedy

What to do — step by step

  1. Stop Using It Now

    Immediately stop using the recalled lip balm as it contains a higher-than-labeled concentration of Octisalate.

Where it went and when

Where it was distributed

Distributed in Colorado.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: yesCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

FDA distribution: “Shipped to one distributer located in Colorado” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Colorado.

Recall timeline

FDA terminated this recall 3.7 years after the firm started it.

1. Firm started the recall: Jun 3, 202012. FDA classified it Class II: Aug 24, 202023. Published in FDA’s Enforcement Report: Sep 2, 202034. FDA terminated the recall: Feb 13, 2024420202024
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

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

✎ GovInfoNow

Questions people ask

What should I do if I have the recalled product?

The manufacturer advises stopping use immediately and contacting them for further guidance.

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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-1540-2020 (June 3, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1540-2020 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