D-37

Active substance: ALUMINUM OXIDE, BRYONIA ALBA ROOT, CITRULLUS COLOCYNTHIS FRUIT PULP, LACHESIS MUTA VENOM, LYCOPODIUM CLAVATUM SPORE, MERCURIC CHLORIDE, STRYCHNOS NUX-VOMICA SEED, LEAD ACETATE ANHYDROUS, SULFUR

SOLUTION · ALUMINUM OXIDE 12 [hp_X]/mL, BRYONIA ALBA ROOT 4 [hp_X]/mL, CITRULLUS COLOCYNTHIS FRUIT PULP 4 [hp_X]/mL, LACHESIS MUTA VENOM 30 [hp_X]/mL, LYCOPODIUM CLAVATUM SPORE 4 [hp_X]/mL, MERCURIC CHLORIDE 8 [hp_X]/mL, STRYCHNOS NUX-VOMICA SEED 6 [hp_X]/mL, LEAD ACETATE ANHYDROUS 12 [hp_X]/mL, SULFUR 12 [hp_X]/mL

United StatesActive

Marketing holder: DNA Labs, Inc.

Verified 2026-10-09 · openFDA NDC

Source: openFDA NDC
Countries with the substance registered: 1

Composition

ALUMINUM OXIDE · 12 [hp_X]/mL
BRYONIA ALBA ROOT · 4 [hp_X]/mL
CITRULLUS COLOCYNTHIS FRUIT PULP · 4 [hp_X]/mL
LACHESIS MUTA VENOM · 30 [hp_X]/mL
LYCOPODIUM CLAVATUM SPORE · 4 [hp_X]/mL
MERCURIC CHLORIDE · 8 [hp_X]/mL
STRYCHNOS NUX-VOMICA SEED · 6 [hp_X]/mL
LEAD ACETATE ANHYDROUS · 12 [hp_X]/mL
SULFUR · 12 [hp_X]/mL

Registration

Registration number: 58264-0037
Registration status: Active
Dispensing: Over the counter
Route: SUBLINGUAL

Sources

product · openFDA NDC · 58264-0037 · Verified 2026-10-09 · open in source
registration_status · openFDA NDC · 58264-0037 · Verified 2026-10-09 · open in source
ingredients.0 · openFDA NDC · 58264-0037 · Verified 2026-10-09 · open in source
ingredients.1 · openFDA NDC · 58264-0037 · Verified 2026-10-09 · open in source
ingredients.2 · openFDA NDC · 58264-0037 · Verified 2026-10-09 · open in source
ingredients.3 · openFDA NDC · 58264-0037 · Verified 2026-10-09 · open in source
ingredients.4 · openFDA NDC · 58264-0037 · Verified 2026-10-09 · open in source
ingredients.5 · openFDA NDC · 58264-0037 · Verified 2026-10-09 · open in source
ingredients.6 · openFDA NDC · 58264-0037 · Verified 2026-10-09 · open in source
ingredients.7 · openFDA NDC · 58264-0037 · Verified 2026-10-09 · open in source
ingredients.8 · openFDA NDC · 58264-0037 · Verified 2026-10-09 · open in source