PURPOSE
Active substance: OCTINOXATE, OCTISALATE, OXYBENZONE
LOTION · OCTINOXATE 7.5 g/100g, OCTISALATE 5 g/100g, OXYBENZONE 3 g/100g
United StatesActive
Marketing holder: Bausch & Lomb Incorporated
Verified 2026-10-09 · openFDA NDC
- Source: openFDA NDC
- Countries with the substance registered: 1
Composition
- OCTINOXATE · 7.5 g/100g
- OCTISALATE · 5 g/100g
- OXYBENZONE · 3 g/100g
Registration
- Registration number
- 24208-001
- Registration status
- Active
- Dispensing
- Over the counter
- Route
- TOPICAL
Sources
- product · openFDA NDC · 24208-001 · Verified 2026-10-09 · open in source
- registration_status · openFDA NDC · 24208-001 · Verified 2026-10-09 · open in source
- ingredients.0 · openFDA NDC · 24208-001 · Verified 2026-10-09 · open in source
- ingredients.1 · openFDA NDC · 24208-001 · Verified 2026-10-09 · open in source
- ingredients.2 · openFDA NDC · 24208-001 · Verified 2026-10-09 · open in source