NDC11 70742028800

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
70742-0288-0	70742-0288
70742-0288-00	70742-0288
70742-288-00	70742-288

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
BODY ACTION PRODUCTS Prolong Lubricating	BENZOCAINE	PRODUCT MAX GROUP INC	3bef5915-1c98-4011-baa9-ad0bbef200c2	2023-11-10	Warnings	Exact identifier ndc (package): 70742-288-00 ndc (product): 70742-288 ndc11 (package): 70742028800

Reported adverse events (FAERS/openFDA)#

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