HIGHFDA DRUG

CA Botana Sunscreen Flawless Skin Fluid Tint SPF 50 Recall 2025

CA Botana International recalls Sunscreen Flawless Skin Fluid Tint SPF 50 after CGMP deviations. The recall covers 1,401 tubes distributed to California, Colorado, Florida, Puerto Rico and Washington. Stop using the product and contact CA Botana for guidance.

Official notice

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DRUG
Recall date
October 10, 2025
Status
ACTIVE
Severity
5/10

Quick Facts at a Glance

Recall Date
October 10, 2025
Hazard Level
HIGH
Brands
CA Botana International, Sunscreen Flawless Skin Fluid Tint
Category
Health & Personal Care
Sold At
Multiple Retailers
Geographic Scope
5 states
At-Risk Groups
GENERAL

What to Do Now

Use this page like a recall checklist: verify the product first, then act on the official remedy.

Immediate steps

  1. 1Stop using the product until you confirm whether it is included in the recall.
  2. 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
  3. 3Follow the official remedy from FDA - Drug Safety; save photos, receipts, labels, and correspondence before contacting the company.
  4. 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.

Check these identifiers

Brand
CA Botana International, Sunscreen Flawless Skin Fluid Tint
Product type
Tinted Moisturizer with SPF 50
Model numbers
Lot Code D54757, exp 3/31/2028, NDC 35192-043-17
UPC codes
35192-043, 35192-043-17
Sizes
2.1 oz / 61 g per tube
Sold at
Multiple Retailers
Where affected
CA, CO, FL, PR, WA

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    October 10, 2025

  2. Reported by FDA DRUG

    December 3, 2025

  3. RecallRadar source check

    April 18, 2026

  4. Consumer action

    Use the official remedy and keep documentation.

Hazard Information

CGMP Deviations

What You Should Do

Consumers and healthcare providers should stop using this product immediately. Contact CA BOTANA International, Inc. or your healthcare provider for guidance. Notification method: Letter

About This Product

This is a tinted moisturizer with SPF 50, containing 21% zinc oxide. It is produced in the United States by CA Botana International.

Why This Is Dangerous

CGMP deviations can affect product quality and safety, potentially leading to inconsistent sun protection or impurities.

Industry Context

This recall is not part of a broader industry pattern.

Real-World Impact

Consumers face a recall for a cosmetic product with potential quality concerns. No injuries have been reported, and refunds or replacements are available.

Practical Guidance

How to identify if yours is affected

  1. Check NDC 35192-043-17 on the product packaging.
  2. Check Lot Code D54757 and expiration date 3/31/2028.
  3. Verify the product was distributed to your state (CA, CO, FL, PR, WA).
  4. If affected, stop use and contact CA Botana for guidance.

Where to find product info

Label on the tube and carton; NDC code and lot/exp date on packaging.

What timeline to expect

Refund or replacement processing may take 4-8 weeks.

If the manufacturer is unresponsive

  • File a complaint with FDA recall portal.
  • Contact your state consumer protection office.
  • Keep records of all correspondence.

How to prevent similar issues

  • Before purchase, check CGMP compliance status and NDC numbers.
  • Choose sunscreen products from reputable brands with clear recall policies.
  • Verify SPF, active ingredients, and packaging integrity.

Documentation advice

Keep photos of packaging, receipts, and all recall communications.

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Product Details

Model numbers: Lot Code D54757; Exp 3/31/2028; NDC: 35192-043-17. Sold in distribution to CA, CO, FL, PR, WA. Quantity: 1,401 tubes. Manufactured by CA Botana International, San Diego, CA 92121. Size: 2.1 oz (61 g) per tube.

Reported Incidents

No injuries or incidents have been reported.

Key Facts

  • Size 2.1 oz / 61 g per tube
  • Lot code D54757
  • Distributed to CA, CO, FL, PR, WA

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: What to Do When You Find a Recalled Product

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Safety Assessment

Risk LevelHIGH
Severity Score
5/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Details

Model Numbers
Lot Code D54757
exp 3/31/2028
NDC 35192-043-17
UPC Codes
35192-043
35192-043-17
Affected States
CA, CO, FL, PR, WA
Report Date
December 3, 2025
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE

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