NDC 87735-002 - SULISRx Sunburn Relief Kit

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC

87735-002

Package NDCs from labels

87735-002-01

Manufacturer

Sephoris Pharmaceuticals, LLC | Blaine Labs, Inc. | Finecure Pharmaceuticals LTD

Effective date

2026-09-19

Current FDA listing

Not matched in FDA.report NDC product tables