NDC 58264-0039

D-39

Lachesis Muta Venom, Lycopodium Clavatum Spore, Palladium, Saxifraga Granulata Whole, And Vespa Crabro

D-39 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; Lycopodium Clavatum Spore; Palladium; Saxifraga Granulata Whole; Vespa Crabro.

• Product ID: 58264-0039_09f8ad4d-eff1-42b6-83f9-3571b0895376
• NDC: 58264-0039
• Product Type: Human Otc Drug
• Proprietary Name: D-39
• Generic Name: Lachesis Muta Venom, Lycopodium Clavatum Spore, Palladium, Saxifraga Granulata Whole, And Vespa Crabro
• 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; LYCOPODIUM CLAVATUM SPORE; PALLADIUM; SAXIFRAGA GRANULATA WHOLE; VESPA CRABRO
• Active Ingredient Strength: 30 [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 58264-0039-1

29.57 mL in 1 BOTTLE, GLASS (58264-0039-1)

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

NDC SPL Data Element Entries

NDC 58264-0039-1 [58264003901]

D-39 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	30 [hp_X]/mL

OpenFDA Data

• SPL SET ID: 0d997878-b973-45aa-a319-9194fcecc5fc
• Manufacturer:
  • DNA Labs, Inc.
• UNII:
  • K3ALM8S49H
  • 5TWQ1V240M
  • VSW71SS07I
  • W1LUS9R48G
  • C88X29Y479