Viscum Tilia Pentas
- Product NDC
- 53645-2750
- 11-digit product format
- 536452750
- Labeler code
- 53645
- Product ID
- 53645-2750_5b871712-535a-eddc-e063-6394a90a4d88
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Viscum album 7X, 11X, 18X, 30X
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- True Botanica, LLC
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2026-09-15
- Substance
- VISCUM ALBUM WHOLE
- Active strength
- 7 [hp_X]/20mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Viscum Tilia Pentas
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| VISCUM ALBUM WHOLE | 7 [hp_X]/20mL |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 53645-2750-4 | 53645275004 | 20 mL in 1 BOTTLE (53645-2750-4) | 20 ml | 2026-09-15 | No | No | Current |