In Your Face Mineral Tint SPF 31, Zinc Oxide 25%, Tinted Sunscreen Broad Spectrum UVA & UVB chemical free, Organic Ingre
Summary
The FDA issued a Class II for In Your Face Mineral Tint SPF 31, Zinc Oxide 25%, Tinted Sunscreen Broad Spectru by KABANA SKIN CARE. Reason: cGMP deviations.
Details
Source
Drug Recall
External ID
D-0515-2025
Action Date
2025-07-16
Status
Ongoing
Category
drug
Product Description
In Your Face Mineral Tint SPF 31, Zinc Oxide 25%, Tinted Sunscreen Broad Spectrum UVA & UVB chemical free, Organic Ingredients, Biodegradable & Baby Safe, 50 mL - 1.7 fl oz per bottle, Manufactured for IN YOUR FACE Skin Care, Belleair Bluffs, FL, Made in USA, NDC: 73369-1601-1
Lot/Code Info: Lot: 408-002
Quantity Affected: 76 bottles
Reason for Recall
cGMP deviations
Distribution
NJ, FL, MI
Type: Voluntary: Firm initiated
Recall Initiated: 2025-03-12
Company
Louisville, CO
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 89 drug recalls issued in the same week, part of 267 drug-related FDA actions this month.
KABANA SKIN CARE has 4 FDA actions in our database, including 4 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (KABANA SKIN CARE) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does KABANA SKIN CARE have FDA actions?
KABANA SKIN CARE has 4 FDA actions in our database, including 4 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "D-0515-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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