NDC 58264-0051

D-51

Atropa Belladonna, Iodine, Lycopus Virginicus, Sodium Chloride, Hekla Lava, And Calcium Hexafluorosilicate

D-51 is a Sublingual Solution in the Human Otc Drug category. It is labeled and distributed by Dna Labs, Inc.. The primary component is Atropa Belladonna; Iodine; Lycopus Virginicus; Sodium Chloride; Hekla Lava; Calcium Hexafluorosilicate.

• Product ID: 58264-0051_b67bcdd8-a3b9-459d-9702-f44a5feee25f
• NDC: 58264-0051
• Product Type: Human Otc Drug
• Proprietary Name: D-51
• Generic Name: Atropa Belladonna, Iodine, Lycopus Virginicus, Sodium Chloride, Hekla Lava, And Calcium Hexafluorosilicate
• 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: ATROPA BELLADONNA; IODINE; LYCOPUS VIRGINICUS; SODIUM CHLORIDE; HEKLA LAVA; CALCIUM HEXAFLUOROSILICATE
• Active Ingredient Strength: 30 [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 58264-0051-1

29.57 mL in 1 BOTTLE, GLASS (58264-0051-1)

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

NDC SPL Data Element Entries

NDC 58264-0051-1 [58264005101]

D-51 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
ATROPA BELLADONNA	30 [hp_X]/mL

OpenFDA Data

• SPL SET ID: 9928dd54-bd3a-47cb-bde5-4bebab3db683
• Manufacturer:
  • DNA Labs, Inc.
• UNII:
  • 2NVP93XVQ3
  • C21158IIRK
  • TWH5125Q6F
  • 451W47IQ8X
  • WQZ3G9PF0H
  • 9679TC07X4