AER Pre-moistened Witch Hazel Pad
Active substance: witch hazel
SOLUTION · WITCH HAZEL 500 mg/mL
United StatesActive
Marketing holder: Birchwood Laboratories LLC
Verified 2026-10-09 · openFDA NDC
- Source: openFDA NDC
Composition
- WITCH HAZEL · 500 mg/mL
Registration
- Registration number
- 50289-3250
- Registration status
- Active
- Dispensing
- Over the counter
- Route
- RECTAL, TOPICAL
Sources
- product · openFDA NDC · 50289-3250 · Verified 2026-10-09 · open in source
- registration_status · openFDA NDC · 50289-3250 · Verified 2026-10-09 · open in source
- ingredients.0 · openFDA NDC · 50289-3250 · Verified 2026-10-09 · open in source