NDC 58264-0050

D-50

Horse Chestnut, Citrullus Colocynthis Fruit Pulp, Black Cohosh, Sodium Chloride, Strychnos Nux-vomica Seed, Phytolacca Americana Root, And Strontium Carbonate

D-50 is a Sublingual Solution in the Human Otc Drug category. It is labeled and distributed by Dna Labs, Inc.. The primary component is Horse Chestnut; Citrullus Colocynthis Fruit Pulp; Black Cohosh; Sodium Chloride; Strychnos Nux-vomica Seed; Phytolacca Americana Root; Strontium Carbonate.

• Product ID: 58264-0050_a2a80b12-54a1-47d8-9697-fd17c55eddf2
• NDC: 58264-0050
• Product Type: Human Otc Drug
• Proprietary Name: D-50
• Generic Name: Horse Chestnut, Citrullus Colocynthis Fruit Pulp, Black Cohosh, Sodium Chloride, Strychnos Nux-vomica Seed, Phytolacca Americana Root, And Strontium Carbonate
• 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: HORSE CHESTNUT; CITRULLUS COLOCYNTHIS FRUIT PULP; BLACK COHOSH; SODIUM CHLORIDE; STRYCHNOS NUX-VOMICA SEED; PHYTOLACCA AMERICANA ROOT; STRONTIUM CARBONATE
• Active Ingredient Strength: 6 [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 58264-0050-1

29.57 mL in 1 BOTTLE, GLASS (58264-0050-1)

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

NDC SPL Data Element Entries

NDC 58264-0050-1 [58264005001]

D-50 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
HORSE CHESTNUT	6 [hp_X]/mL

OpenFDA Data

• SPL SET ID: df118b9b-dee7-4555-bcae-751007c1fd2c
• Manufacturer:
  • DNA Labs, Inc.
• UNII:
  • 23H32AOH17
  • 3C18L6RJAZ
  • 451W47IQ8X
  • 11E6VI8VEG
  • K73E24S6X9
  • 269XH13919
  • 41YPU4MMCA