NDC 58264-0108

D-102

Garlic, Aloe, Mycobacterium Tuberculosis, Eucalyptus Globulus Leaf, Canis Lupus Familiaris Milk, Cow Milk, Rancid Beef, Delphinium Staphisagria Seed, Staphylococcus Epidermidis, Staphylococcus Haemolyticus, Staphylococcus Simulans, Streptococcus Pyogenes, And Sulfur

D-102 is a Sublingual Solution in the Human Otc Drug category. It is labeled and distributed by Dna Labs, Inc.. The primary component is Garlic; Aloe; Mycobacterium Tuberculosis; Eucalyptus Globulus Leaf; Canis Lupus Familiaris Milk; Cow Milk; Rancid Beef; Delphinium Staphisagria Seed; Staphylococcus Epidermidis; Staphylococcus Haemolyticus; Staphylococcus Simulans; Streptococcus Pyogenes; Sulfur.

• Product ID: 58264-0108_9b00d0f8-259b-456e-8b79-25a9f238e441
• NDC: 58264-0108
• Product Type: Human Otc Drug
• Proprietary Name: D-102
• Generic Name: Garlic, Aloe, Mycobacterium Tuberculosis, Eucalyptus Globulus Leaf, Canis Lupus Familiaris Milk, Cow Milk, Rancid Beef, Delphinium Staphisagria Seed, Staphylococcus Epidermidis, Staphylococcus Haemolyticus, Staphylococcus Simulans, Streptococcus Pyogenes, And Sulfur
• 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: GARLIC; ALOE; MYCOBACTERIUM TUBERCULOSIS; EUCALYPTUS GLOBULUS LEAF; CANIS LUPUS FAMILIARIS MILK; COW MILK; RANCID BEEF; DELPHINIUM STAPHISAGRIA SEED; STAPHYLOCOCCUS EPIDERMIDIS; STAPHYLOCOCCUS HAEMOLYTICUS; STAPHYLOCOCCUS SIMULANS; STREPTOCOCCUS PYOGENES; SULFUR
• 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; [hp_X]/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 58264-0108-1

29.57 mL in 1 BOTTLE, GLASS (58264-0108-1)

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

NDC SPL Data Element Entries

NDC 58264-0108-1 [58264010801]

D-102 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
GARLIC	12 [hp_X]/mL

OpenFDA Data

• SPL SET ID: d64022f6-e3e1-459b-b896-843c2a92d9da
• Manufacturer:
  • DNA Labs, Inc.
• UNII:
  • 092IJ99835
  • R0EM8D5HFD
  • 29SUH5R3HU
  • V5VD430YW9
  • 70FD1KFU70
  • LJ2LP0YL98
  • V1V998DC17
  • G39P120JQT
  • D5T403TNGE
  • S546YLW6E6
  • V68E0X60VL
  • 00543AP1JV
  • 917J3173FT