NDC11 14222213104

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 NDCProduct root
14222-2131-0414222-2131
14222-2131-414222-2131

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 ยท 2 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
UNBLEMISH 30-Day RegimenSALICYLIC ACID, BENZOYL PEROXIDE, HOMOSALATE, OCTOCRYLENE, OCTISALATE, AVOBENZONERodan & Fieldse9a52ccc-6ba0-4417-86cc-b2116a5b8d262026-04-01WarningsExact identifier
ndc (package): 14222-2131-4
ndc11 (package): 14222213104
UNBLEMISH Invisible Matte DefenseHOMOSALATE, OCTOCRYLENE, OCTISALATE, AVOBENZONERodan & Fields9dfe7d50-f347-4671-9657-5e4fbe42b4412023-11-27WarningsExact identifier
ndc (product): 14222-2131

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.