LINDEN FLOWER TINC
- Product NDC
- 44911-0221
- 11-digit product format
- 449110221
- Labeler code
- 44911
- Product ID
- 44911-0221_752aec9d-c120-4706-8e62-53ef82d979f4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Tilia europaea
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Energique, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2015-07-16
- Substance
- TILIA X EUROPAEA FLOWER
- 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
- LINDEN FLOWER TINC
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| TILIA X EUROPAEA FLOWER | 1 [hp_X]/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | NHV2K1OUDH |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 44911-0221-1 | LINDEN FLOWER TINC | 30 mL in 1 BOTTLE, DROPPER | LIQUID | 30 | | 4 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 44911-0221 | LINDEN FLOWER TINC (TILIA EUROPAEA) LIQUID [ENERGIQUE, INC.] | 4 | Current NDC, Legacy NDC, 1 package rows | 20241030_f2ad2046-1eff-4fa0-b6a8-9c6b00d09c06.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 44911-0221-1 | 44911022101 | 30 mL in 1 BOTTLE, DROPPER (44911-0221-1) | 30 ml | 2015-07-16 | 0000-00-00 | No | No | Current |