NDC 58264-0382

G-19

Ilex Aquifolium Leaf

G-19 is a Sublingual Solution in the Human Otc Drug category. It is labeled and distributed by Dna Labs, Inc.. The primary component is Ilex Aquifolium Leaf.

• Product ID: 58264-0382_2ed771ab-1914-49f7-a2af-6f0d28e02e62
• NDC: 58264-0382
• Product Type: Human Otc Drug
• Proprietary Name: G-19
• Generic Name: Ilex Aquifolium Leaf
• 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: ILEX AQUIFOLIUM LEAF
• Active Ingredient Strength: 1 [hp_X]/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 58264-0382-2

59.14 mL in 1 BOTTLE, GLASS (58264-0382-2)

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

NDC SPL Data Element Entries

NDC 58264-0382-2 [58264038202]

G-19 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
ILEX AQUIFOLIUM LEAF	1 [hp_X]/mL

OpenFDA Data

• SPL SET ID: 411fd7e6-1a91-4d19-b394-c713c88e2130
• Manufacturer:
  • DNA Labs, Inc.
• UNII:
  • 9Z32IEA9F7