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MEB PainGuard Patch

Active substance: CALCIUM SILICATE, MANGANESE, FERRIC CHLORIDE HEXAHYDRATE, SODIUM NITRATE, FERROSOFERRIC PHOSPHATE, CALCIUM FLUORIDE, KAOLIN, VANADIUM, ZINC, MAGNESIUM CHLORIDE, SULFUR

PATCH · CALCIUM SILICATE 5 [hp_X]/12[hp_X], MANGANESE 12 [hp_X]/12[hp_X], FERRIC CHLORIDE HEXAHYDRATE 7 [hp_X]/12[hp_X], SODIUM NITRATE 5 [hp_X]/12[hp_X], FERROSOFERRIC PHOSPHATE 7 [hp_X]/12[hp_X], CALCIUM FLUORIDE 6 [hp_X]/12[hp_X], KAOLIN 5 [hp_X]/12[hp_X], VANADIUM 12 [hp_X]/12[hp_X], ZINC 8 [hp_X]/12[hp_X], MAGNESIUM CHLORIDE 7 [hp_X]/12[hp_X], SULFUR 4 [hp_X]/12[hp_X]

United StatesActive

Marketing holder: Kadesh Incoporation Co,Ltd

Verified 2026-10-09 · openFDA NDC

Composition
Registration
Registration number
81488-011
Registration status
Active
Dispensing
Over the counter
Route
TRANSDERMAL
Sources
  • product · openFDA NDC · 81488-011 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 81488-011 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 81488-011 · Verified 2026-10-09 · open in source
  • ingredients.1 · openFDA NDC · 81488-011 · Verified 2026-10-09 · open in source
  • ingredients.2 · openFDA NDC · 81488-011 · Verified 2026-10-09 · open in source
  • ingredients.3 · openFDA NDC · 81488-011 · Verified 2026-10-09 · open in source
  • ingredients.4 · openFDA NDC · 81488-011 · Verified 2026-10-09 · open in source
  • ingredients.5 · openFDA NDC · 81488-011 · Verified 2026-10-09 · open in source
  • ingredients.6 · openFDA NDC · 81488-011 · Verified 2026-10-09 · open in source
  • ingredients.7 · openFDA NDC · 81488-011 · Verified 2026-10-09 · open in source
  • ingredients.8 · openFDA NDC · 81488-011 · Verified 2026-10-09 · open in source
  • ingredients.9 · openFDA NDC · 81488-011 · Verified 2026-10-09 · open in source
  • ingredients.10 · openFDA NDC · 81488-011 · Verified 2026-10-09 · open in source