NDC11 49404015401

This exact 11-digit normalized identifier can correspond to more than one FDA hyphenation. FDA.report preserves the exact identifier and exposes every structurally valid candidate without guessing.

Possible FDA NDC forms#

Package NDC, Product root table
Package NDC	Product root
49404-0154-01	49404-0154
49404-0154-1	49404-0154
49404-154-01	49404-154

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown 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
DR.JART EVERY SUN DAY SUN FLUID	HOMOSALATE, OCTINOXATE, OCTISALATE, OCTOCRYLENE, AVOBENZONE	Have & Be Co., Ltd.	f06d8f90-f3df-6d76-e053-2a95a90af1f8	2025-01-24	Warnings	Exact identifier ndc (package): 49404-154-01 ndc (product): 49404-154 ndc11 (package): 49404015401