Viscum Populus RK 23X
- Product NDC
- 53645-2191
- 11-digit product format
- 536452191
- Labeler code
- 53645
- Product ID
- 53645-2191_2cca1ee3-3df4-7703-e063-6394a90a013a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Viscum Populus RK 23X
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- True Botanica, LLC
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2025-06-02
- Substance
- VISCUM ALBUM WHOLE
- Active strength
- 23 [hp_X]/20mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Viscum Populus RK 23X
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| VISCUM ALBUM WHOLE | 23 [hp_X]/20mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | E6839Q6DO1 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 53645-2191-4 | Viscum Populus RK 23X | 20 mL in 1 BOTTLE | LIQUID | 20 | | 1 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 53645-2191-4 | 53645219104 | 20 mL in 1 BOTTLE (53645-2191-4) | 20 ml | 2025-06-02 | No | No | Historical |