G-18
- Product NDC
- 58264-0381
- 11-digit product format
- 582640381
- Labeler code
- 58264
- Product ID
- 58264-0381_2b532077-bbdb-534d-e063-6394a90a4a26
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- FRAXINUS EXCELSIOR LEAF
- Dosage form
- SOLUTION
- Route
- SUBLINGUAL
- Labeler
- DNA Labs, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 1990-01-01
- Substance
- FRAXINUS EXCELSIOR LEAF
- Active strength
- 1 [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- G-18
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| FRAXINUS EXCELSIOR LEAF | 1 [hp_X]/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | RC38362Q7M |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 58264-0381-2 | G-18 | 59.14 mL in 1 BOTTLE, GLASS | SOLUTION | 59.14 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 58264-0381 | G-18 (FRAXINUS EXCELSIOR LEAF) SOLUTION [DNA LABS, INC.] | 3 | Current NDC, Legacy NDC, 1 package rows | 20250112_8f21c2a7-825c-44de-9341-8a66b2c0e08a.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 58264-0381-2 | 58264038102 | 59.14 mL in 1 BOTTLE, GLASS (58264-0381-2) | 59.14 ml | 1990-01-01 | 0000-00-00 | No | No | Current |