D-100
- Product NDC
- 58264-0106
- 11-digit product format
- 582640106
- Labeler code
- 58264
- Product ID
- 58264-0106_2b9ec3e6-b13c-d877-e063-6294a90ad789
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Fucus vesiculosus
- Dosage form
- SOLUTION
- Route
- SUBLINGUAL
- Labeler
- DNA Labs, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 1990-01-01
- Substance
- FUCUS VESICULOSUS
- Active strength
- 3 [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
- D-100
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| FUCUS VESICULOSUS | 3 [hp_X]/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 535G2ABX9M |
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 58264-0106-1 | D-100 | 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 |
|---|
| 58264-0106 | D-100 (FUCUS VESICULOSUS) SOLUTION [DNA LABS, INC.] | 3 | Current NDC, Legacy NDC, 1 package rows | 20250115_0a2aed6f-6e1c-43e4-b5df-1dc73d7e6f2b.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 58264-0106-1 | 58264010601 | 29.57 mL in 1 BOTTLE, GLASS (58264-0106-1) | 29.57 ml | 1990-01-01 | 0000-00-00 | No | No | Current |