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FDA Import Refusal 144-2947849-1/1/1 — Wyeth Consumer Healthcare

Wyeth Consumer Healthcare — FEI 3003851828

The FDA refused shipment 144-2947849-1/1/1 from Wyeth Consumer Healthcare (United States) on Feb 1, 2010. The refused product falls under Drugs and Biologics — OXYBENZONE (ULTRAVIOLET SCREEN/SUNSCREEN). Cited charges: 118,178 This firm has 3 other import refusals on record.

Refusal details

Date
Feb 1, 2010
Country
United States
Product Category
Drugs and Biologics
Product Code
66PBJ07 OXYBENZONE (ULTRAVIOLET SCREEN/SUNSCREEN)
Charges
118,178

Other import refusals

FDA data resources

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