A-30
- Product NDC
- 58264-0322
- 11-digit product format
- 582640322
- Labeler code
- 58264
- Product ID
- 58264-0322_2b50cd9c-dbe2-df72-e063-6394a90a53ee
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- TOBACCO LEAF
- Dosage form
- SOLUTION
- Route
- SUBLINGUAL
- Labeler
- DNA Labs, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 1990-01-01
- Substance
- TOBACCO LEAF
- Active strength
- 30 [hp_X]/mL
- Pharmacologic classes
- Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- A-30
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| TOBACCO LEAF | 30 [hp_X]/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 6YR2608RSU |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 58264-0322-1 | A-30 | 29.57 mL in 1 BOTTLE, GLASS | SOLUTION | 29.57 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 58264-0322 | A-30 (TOBACCO LEAF) SOLUTION [DNA LABS, INC.] | 3 | Current NDC, Legacy NDC, 1 package rows | 20250112_62aab64a-7cb7-46c1-9886-ee0c7ffd0b13.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 58264-0322-1 | 58264032201 | 29.57 mL in 1 BOTTLE, GLASS (58264-0322-1) | 29.57 ml | 1990-01-01 | 0000-00-00 | No | No | Current |