NDC11 42851009006

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
42851-0090-06	42851-0090
42851-0090-6	42851-0090
42851-090-06	42851-090

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 · 2 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
ZO Skin Health Post Procedure Program	ALUMINUM ACETATE	ZO Skin Health, Inc.	9786acc8-06ae-4f2b-9602-b7e8c3baeca5	2024-11-12	Warnings	Exact identifier ndc (package): 42851-090-06 ndc11 (package): 42851009006
ZO Skin Health Astringent Solution	ALUMINUM ACETATE	ZO Skin Health, Inc.	cb801d7e-52ad-6c16-e053-2a95a90a7a1f	2024-10-31	Warnings	Exact identifier ndc (package): 42851-090-06 ndc (product): 42851-090 ndc11 (package): 42851009006

Reported adverse events (FAERS/openFDA)#

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