Baptisia Tinctoria Kit Refill
- Product NDC
- 71919-765
- 11-digit product format
- 719190765
- Labeler code
- 71919
- Product ID
- 71919-765_2cc7eaaf-e2c6-f06a-e063-6394a90a1961
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- BAPTISIA TINCTORIA ROOT
- Dosage form
- PELLET
- Route
- ORAL
- Labeler
- Washington Homeopathic Products
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2022-05-10
- Substance
- BAPTISIA TINCTORIA ROOT
- Active strength
- 200 [hp_C]/1
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Baptisia Tinctoria Kit Refill
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BAPTISIA TINCTORIA ROOT | 200 [hp_C]/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 5EF0HWI5WU |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71919-765-01 | Baptisia Tinctoria Kit Refill | 350 in 1 VIAL, GLASS | PELLET | 350 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71919-765 | BAPTISIA TINCTORIA KIT REFILL (BAPTISIA TINCTORIA ROOT) PELLET [WASHINGTON HOMEOPATHIC PRODUCTS] | 4 | Current NDC, Legacy NDC, 1 package rows | 20250130_dead18ed-a4ba-8129-e053-2a95a90a3f2e.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71919-765-01 | 71919076501 | 350 PELLET in 1 VIAL, GLASS (71919-765-01) | 350 pellet | 2022-05-10 | 0000-00-00 | No | No | Current |