NDC11 70157002705

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
70157-0027-05	70157-0027
70157-0027-5	70157-0027
70157-027-05	70157-027

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
Standard Procedure SPF 50 Sunscreen Face and Body	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Baxter Laboratories	34f6150d-9627-94a5-e063-6394a90ad448	2026-05-13	Warnings	Exact identifier ndc (package): 70157-027-05 ndc (product): 70157-027 ndc11 (package): 70157002705

Reported adverse events (FAERS/openFDA)#

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