NDC11 10742100201

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
10742-1002-01	10742-1002
10742-1002-1	10742-1002

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
Oxy Maximum Strength Rapid Spot Treatment	OXY MAXIMUM STRENGTH RAPID SPOT TREATMENT	The Mentholatum Company	28886273-a71a-46ea-e063-6394a90ac11d	2024-12-05	Warnings	Exact identifier ndc (package): 10742-1002-1 ndc (product): 10742-1002 ndc11 (package): 10742100201