NDC 58264-0118

D-112

Lachesis Muta Venom, Silicon Dioxide, Sodium Chloride, Ranunculus Bulbosus, Aconitum Napellus, Activated Charcoal, Nitroglycerin, Oyster Shell Calcium Carbonate, Crude, Anemone Pratensis, Plantago Major, Arsenic Trioxide, And Magnesium Phosphate, Dibasic Trihydrate

D-112 is a Sublingual Solution in the Human Otc Drug category. It is labeled and distributed by Dna Labs, Inc.. The primary component is Lachesis Muta Venom; Silicon Dioxide; Sodium Chloride; Ranunculus Bulbosus; Aconitum Napellus; Activated Charcoal; Nitroglycerin; Oyster Shell Calcium Carbonate, Crude; Anemone Pratensis; Plantago Major; Arsenic Trioxide; Magnesium Phosphate, Dibasic Trihydrate.

• Product ID: 58264-0118_5a46b7c0-d8e3-47b3-9022-f61256c99965
• NDC: 58264-0118
• Product Type: Human Otc Drug
• Proprietary Name: D-112
• Generic Name: Lachesis Muta Venom, Silicon Dioxide, Sodium Chloride, Ranunculus Bulbosus, Aconitum Napellus, Activated Charcoal, Nitroglycerin, Oyster Shell Calcium Carbonate, Crude, Anemone Pratensis, Plantago Major, Arsenic Trioxide, And Magnesium Phosphate, Dibasic Trihydrate
• Dosage Form: Solution
• Route of Administration: SUBLINGUAL
• Marketing Start Date: 1990-01-01
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: DNA Labs, Inc.
• Substance Name: LACHESIS MUTA VENOM; SILICON DIOXIDE; SODIUM CHLORIDE; RANUNCULUS BULBOSUS; ACONITUM NAPELLUS; ACTIVATED CHARCOAL; NITROGLYCERIN; OYSTER SHELL CALCIUM CARBONATE, CRUDE; ANEMONE PRATENSIS; PLANTAGO MAJOR; ARSENIC TRIOXIDE; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE
• Active Ingredient Strength: 12 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 58264-0118-1

29.57 mL in 1 BOTTLE, GLASS (58264-0118-1)

• Marketing Start Date: 1990-01-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 58264-0118-1 [58264011801]

D-112 SOLUTION

• Marketing Category: UNAPPROVED HOMEOPATHIC
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 1990-01-01
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
LACHESIS MUTA VENOM	12 [hp_X]/mL

OpenFDA Data

• SPL SET ID: 8d517ef2-3a1e-4393-9452-a4cd0f0a3bca
• Manufacturer:
  • DNA Labs, Inc.
• UNII:
  • 8E272251DI
  • ETJ7Z6XBU4
  • S7V92P67HO
  • AEQ8NXJ0MB
  • VSW71SS07I
  • 451W47IQ8X
  • 2E32821G6I
  • HF539G9L3Q
  • W2469WNO6U
  • G59M7S0WS3
  • 2P3VWU3H10
  • U0NQ8555JD