NDC11 70742029200

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
70742-0292-0	70742-0292
70742-0292-00	70742-0292
70742-292-00	70742-292

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 Higher Control Male Climax	BENZOCAINE	PRODUCT MAX GROUP INC	3c7fa73b-abe8-4a8d-951c-4e785d6e812c	2023-11-10	Warnings	Exact identifier ndc (package): 70742-292-00 ndc (product): 70742-292 ndc11 (package): 70742029200

Reported adverse events (FAERS/openFDA)#

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