NDC 58264-0322

A-30

Tobacco Leaf

A-30 is a Sublingual Solution in the Human Otc Drug category. It is labeled and distributed by Dna Labs, Inc.. The primary component is Tobacco Leaf.

• Product ID: 58264-0322_db9e4c3f-ca69-41bb-b9fd-e87205aad277
• NDC: 58264-0322
• Product Type: Human Otc Drug
• Proprietary Name: A-30
• Generic Name: Tobacco 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: TOBACCO LEAF
• Active Ingredient Strength: 30 [hp_X]/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 58264-0322-1

29.57 mL in 1 BOTTLE, GLASS (58264-0322-1)

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

NDC SPL Data Element Entries

NDC 58264-0322-1 [58264032201]

A-30 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
TOBACCO LEAF	30 [hp_X]/mL

OpenFDA Data

• SPL SET ID: 62aab64a-7cb7-46c1-9886-ee0c7ffd0b13
• Manufacturer:
  • DNA Labs, Inc.
• UNII:
  • 6YR2608RSU

NDC Crossover Matching brand name "A-30" or generic name "Tobacco Leaf"

NDC	Brand Name	Generic Name
58264-0322	A-30	TOBACCO LEAF
64117-993	Motion Sickness 1	TOBACCO LEAF
0220-4906	Tabacum	TOBACCO LEAF
0220-4907	Tabacum	TOBACCO LEAF
0220-4908	Tabacum	TOBACCO LEAF
0220-4909	Tabacum	TOBACCO LEAF
0220-4910	Tabacum	TOBACCO LEAF
0220-4911	Tabacum	TOBACCO LEAF
0220-4916	Tabacum	TOBACCO LEAF
68428-661	Tabacum	TOBACCO LEAF
36987-2238	Tobacco Leaf	Tobacco Leaf
36987-2239	Tobacco Leaf	Tobacco Leaf
36987-2240	Tobacco Leaf	Tobacco Leaf
36987-2242	Tobacco Leaf	Tobacco Leaf
36987-2244	Tobacco Leaf	Tobacco Leaf
36987-2245	Tobacco Leaf	Tobacco Leaf
49643-022	Tobacco Leaf	Tobacco Leaf