NDC11 87170001004

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
87170-0010-04	87170-0010
87170-0010-4	87170-0010
87170-010-04	87170-010

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
HAMPTON SUN SPF50 SUNSHIELD BODY GLOW	HOMOSALATE 10% OCTOCRYLENE 10% AVOBENZONE 3% OCTICALATE 5%	S&C Hampton Sun LLC	26190992-9463-47ae-86a5-0dbc05be8773	2026-02-02	Warnings	Exact identifier ndc (package): 87170-010-04 ndc (product): 87170-010 ndc11 (package): 87170001004

Reported adverse events (FAERS/openFDA)#

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