# SULISRx Sunburn Relief Kit

NDC: 87735-003
Generic name: Sunburn Relief Kit
Labeler / Manufacturer: Sephoris Pharmaceuticals, LLC
Product type: HUMAN OTC DRUG
Marketing category: Unapproved drug (not FDA-reviewed)
Dosage form: KIT
Routes: —
Marketing started: 20260903



## Active ingredients

—

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"87735-003"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=87735-003