B03 Sinus Relief

Active substance: LACTOSE, UNSPECIFIED FORM, THUJA OCCIDENTALIS LEAFY TWIG, POTASSIUM SULFATE, GOLDENSEAL, POTASSIUM DICHROMATE, POTASSIUM CHLORIDE, PULSATILLA VULGARIS, PHOSPHORUS, SKIM MILK, CALCIUM IODIDE, ECHINACEA ANGUSTIFOLIA, ECHINACEA PURPUREA, EUPHORBIA RESINIFERA RESIN, CALCIUM SULFIDE, HISTAMINE DIHYDROCHLORIDE, MERCURIC SULFIDE, ONION, CALCIUM SULFATE ANHYDROUS, LUFFA OPERCULATA FRUIT

SOLUTION/ DROPS · LACTOSE, UNSPECIFIED FORM 12 [hp_X]/mL, THUJA OCCIDENTALIS LEAFY TWIG 10 [hp_X]/mL, POTASSIUM SULFATE 12 [hp_X]/mL, GOLDENSEAL 1 [hp_X]/mL, POTASSIUM DICHROMATE 15 [hp_X]/mL, POTASSIUM CHLORIDE 10 [hp_X]/mL, PULSATILLA VULGARIS 12 [hp_X]/mL, PHOSPHORUS 8 [hp_X]/mL, SKIM MILK 30 [hp_X]/mL, CALCIUM IODIDE 12 [hp_X]/mL, ECHINACEA ANGUSTIFOLIA 1 [hp_X]/mL, ECHINACEA PURPUREA 1 [hp_X]/mL, EUPHORBIA RESINIFERA RESIN 6 [hp_X]/mL, CALCIUM SULFIDE 15 [hp_X]/mL, HISTAMINE DIHYDROCHLORIDE 30 [hp_X]/mL, MERCURIC SULFIDE 12 [hp_X]/mL, ONION 12 [hp_X]/mL, CALCIUM SULFATE ANHYDROUS 12 [hp_X]/mL, LUFFA OPERCULATA FRUIT 12 [hp_X]/mL

United StatesActive

Marketing holder: Apex Energetics Inc.

Verified 2026-10-09 · openFDA NDC

Source: openFDA NDC
Countries with the substance registered: 1

Composition

LACTOSE, UNSPECIFIED FORM · 12 [hp_X]/mL
THUJA OCCIDENTALIS LEAFY TWIG · 10 [hp_X]/mL
POTASSIUM SULFATE · 12 [hp_X]/mL
GOLDENSEAL · 1 [hp_X]/mL
POTASSIUM DICHROMATE · 15 [hp_X]/mL
POTASSIUM CHLORIDE · 10 [hp_X]/mL
PULSATILLA VULGARIS · 12 [hp_X]/mL
PHOSPHORUS · 8 [hp_X]/mL
SKIM MILK · 30 [hp_X]/mL
CALCIUM IODIDE · 12 [hp_X]/mL
ECHINACEA ANGUSTIFOLIA · 1 [hp_X]/mL
ECHINACEA PURPUREA · 1 [hp_X]/mL
EUPHORBIA RESINIFERA RESIN · 6 [hp_X]/mL
CALCIUM SULFIDE · 15 [hp_X]/mL
HISTAMINE DIHYDROCHLORIDE · 30 [hp_X]/mL
MERCURIC SULFIDE · 12 [hp_X]/mL
ONION · 12 [hp_X]/mL
CALCIUM SULFATE ANHYDROUS · 12 [hp_X]/mL
LUFFA OPERCULATA FRUIT · 12 [hp_X]/mL

Registration

Registration number: 63479-0203
Registration status: Active
Dispensing: Over the counter
Route: SUBLINGUAL

Sources

product · openFDA NDC · 63479-0203 · Verified 2026-10-09 · open in source
registration_status · openFDA NDC · 63479-0203 · Verified 2026-10-09 · open in source
ingredients.0 · openFDA NDC · 63479-0203 · Verified 2026-10-09 · open in source
ingredients.1 · openFDA NDC · 63479-0203 · Verified 2026-10-09 · open in source
ingredients.2 · openFDA NDC · 63479-0203 · Verified 2026-10-09 · open in source
ingredients.3 · openFDA NDC · 63479-0203 · Verified 2026-10-09 · open in source
ingredients.4 · openFDA NDC · 63479-0203 · Verified 2026-10-09 · open in source
ingredients.5 · openFDA NDC · 63479-0203 · Verified 2026-10-09 · open in source
ingredients.6 · openFDA NDC · 63479-0203 · Verified 2026-10-09 · open in source
ingredients.7 · openFDA NDC · 63479-0203 · Verified 2026-10-09 · open in source
ingredients.8 · openFDA NDC · 63479-0203 · Verified 2026-10-09 · open in source
ingredients.9 · openFDA NDC · 63479-0203 · Verified 2026-10-09 · open in source
ingredients.10 · openFDA NDC · 63479-0203 · Verified 2026-10-09 · open in source
ingredients.11 · openFDA NDC · 63479-0203 · Verified 2026-10-09 · open in source
ingredients.12 · openFDA NDC · 63479-0203 · Verified 2026-10-09 · open in source
ingredients.13 · openFDA NDC · 63479-0203 · Verified 2026-10-09 · open in source
ingredients.14 · openFDA NDC · 63479-0203 · Verified 2026-10-09 · open in source
ingredients.15 · openFDA NDC · 63479-0203 · Verified 2026-10-09 · open in source
ingredients.16 · openFDA NDC · 63479-0203 · Verified 2026-10-09 · open in source
ingredients.17 · openFDA NDC · 63479-0203 · Verified 2026-10-09 · open in source
ingredients.18 · openFDA NDC · 63479-0203 · Verified 2026-10-09 · open in source