NDC 72203-011-01

This exact product or package identity exists in FDA auxiliary data but is not present in the current primary NDC product table. The package identity is preserved; status rows are reported source observations, not medical conclusions.

Requested NDC: 72203-011-01
Product root: 72203-011
Identity scope: Package
Primary current NDC product row: Not present

NDC auxiliary status#

Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status. Browse every current auxiliary row, including rows without a usable NDC. · Browse every captured source and parsed snapshot.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	72203-011	72203-011-01	D	Discontinued by firm		2026-08-03

openFDA label cross-check#

Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report. Every label matching the complete exact-identifier union is deduplicated and paginated below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
COVER plus CORRECT/TINTED MOISTURIZER CC CRM FAIR	OCTINOXATE, OCTISALATE, OXYBENZONE, AND TITANIUM DIOXIDE	Bluemercury	5c590aed-d2f2-4478-8919-37c848752b42	2025-01-29	Warnings	Exact identifier ndc (package): 72203-011-01 ndc (product): 72203-011 ndc11 (package): 72203001101