CBI Laboratories, Inc. recalls Advanced Protection Sunscreen spf 30 (Octinoxate 7.5%, Octisalate 5%, Oxybenzone 6%), 4.5 Oz/127.5 g tube.
CBI Laboratories recalls SPF 30 sunscreen with incorrect active ingredient percentages. Products may not provide intended protection. Consumers should contact the company for details.
Lower-risk recall
Subpotent Drug:Out of specification for percentage of active pharmaceutical ingredients.
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What happened, in plain English
CBI Laboratories is recalling SPF 30 sunscreen products that have incorrect levels of active ingredients. This means the sunscreen may not provide the promised protection from the sun. Read more at govinfonow.com/recall/39374-cbi-laboratories-recalls-spf-30-sunscreen-due-to-incorrect-ingredient.
Source Summary by GovInfoNow · govinfonow.com/recall/39374-cbi-laboratories-recalls-spf-30-sunscreen-due-to-incorrect-ingredient · Updated October 5, 2026 · FDA enforcement record: FDA #D-0341-2019
Cite this page
“CBI Laboratories Recalls SPF 30 Sunscreen Due to Incorrect Ingredient Levels.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/39374-cbi-laboratories-recalls-spf-30-sunscreen-due-to-incorrect-ingredient. Based on FDA recall #D-0341-2019 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0341-2019%22&limit=1).
Why it’s dangerous
The sunscreen contains incorrect percentages of active ingredients, meaning it may not provide the intended sun protection. This could lead to inadequate protection from UV rays, especially for people with sensitive skin or high sun exposure.
Who’s affected
People who own or use the recalled sunscreen products are affected. Those with sensitive skin or high sun exposure risk may be at slightly higher risk.
How to tell if you have this one
Check for the product name 'Advanced Protection Sunscreen SPF 30' and the lot numbers listed in the recall notice. The products were sold between 2018 and 2020.
- Brand
CBI Laboratories- Category
Drug
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class III- Status
Terminated- Distribution
United States, Maldives, Canada, United Arab Emirates, and New Zealand
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| D-0341-2019 | Advanced Protection Sunscreen spf 30 (Octinoxate 7.5%, Octisalate 5%, Oxybenzone 6%), 4.5 Oz/127.5 g tube.; Lot #: 131965, Exp 12/2018; 127426 Exp. 01/2019; 129045, 130424 Exp. 06/2019; 130432 Exp. 10/2019; 131870 Exp. 06/2019; 132648, Exp. 03/2020; 133732 Exp. 04/2020; 134400 Exp. 02/2020; 135345 Exp. 08/2020 | 5363 tubes |
| D-0342-2019 | Options Rx Anti-Oxidant Oil-Free Sunscreeen (Octinoxate 7.5%, Octisalate 5%, Oxybenzone 6%), 4.5 oz./128 g tube, Mfg. For Credentials Skincare Fort Worth, TX 76155; Lot #: 129114 Exp. 06/2019; 131927,133239 Exp. 03/2020; 126292, Exp.01/2019. | 2055 tubes |
What to do — step by step
Check Product Details
Look for the lot numbers listed in the recall notice to confirm if your sunscreen is affected.
Questions people ask
Is this sunscreen dangerous?
The sunscreen may not provide the intended sun protection due to incorrect ingredient levels, but it is not considered a serious health hazard.
How do I know if my sunscreen is recalled?
Check for the lot numbers listed in the recall notice: 131965, 127426, 129045, 130424, 130432, 131870, 132648, 133732, 134400, 135345.
What should I do if I have the recalled sunscreen?
The recall notice does not specify a remedy, so contact CBI Laboratories for further instructions.
Contact CBI Laboratories
We’ve drafted a message you can send CBI Laboratories to request your refund or repair — edit it as you like.
Subject: Recall D-0341-2019 — CBI Laboratories CBI Laboratories Hello, I own a CBI Laboratories that is covered by recall D-0341-2019 from CBI Laboratories. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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-0341-2019 (December 10, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0341-2019 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.