FDA Import Refusal 8L5-0002450-6/421/2 — AMERICAN REGIONAL LLC

AMERICAN REGIONAL LLC — FEI 3033050640

The FDA refused shipment 8L5-0002450-6/421/2 from AMERICAN REGIONAL LLC (United States) on Jan 8, 2025. The refused product falls under Drugs and Biologics — OCTINOXATE (ULTRAVIOLET SCREEN/SUNSCREEN). Cited charges: 118,3280

Refusal details

Date
Jan 8, 2025
Country
United States
Product Category
Drugs and Biologics
Product Code
66PDY14 OCTINOXATE (ULTRAVIOLET SCREEN/SUNSCREEN)
Charges
118,3280

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.