Mistletoe Herb Strawberry Flavor
100/100
This product looks safe
- No ingredients exceed tolerable upper intake levels
- 100% of ingredients have research evidence
A
Label Compliance Grade
Product Label
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Label Data
25 Drop(s)
Serving Size
227
Servings
Botanical
Product Type
100%
Evidence Coverage
Supplement Facts — Evidence Check
📊 Market median: 500.0mg (32 products)
📚 9 studies (Tier A: 0, B: 2)
Other Ingredients
Glycerin
Strawberry flavor
Label Claims — Verification
❓
All Other
All Other (97% of products)
Structure/Function (74% of products)
Target Groups
Adult (18 - 50 Years)
Product Information
📋 Directions for Use
Suggested Use: Take 25-40 drops of extract in a small amount of warm water 3-4 times daily. Shake well before using.
⚠️ Warnings & Precautions
Keep away from children.
Do not use if safety seal around cap is broken or missing.
🧪 Formulation Notes
Glycerite liquid extract (1:5)
Alcohol free
Product Details
Research Evidence
10
Research Sources
52
Avg Quality Score
5
Meta Analysis
3
Rct
1
Systematic Review
1
Other
B
Cancer-related fatigue in patients treated with mistletoe extracts: a systematic review and meta-analysis
B
A Systematic Review and Meta-Analysis on the Survival of Cancer Patients Treated with a Fermented Viscum album L. Extract (Iscador): An Update of Findings
C
Survival of cancer patients treated with mistletoe extract (Iscador): a systematic literature review
C
Mistletoe Extract in Patients With Advanced Pancreatic Cancer: a Double-Blind, Randomized, Placebo-Controlled Tial (MISTRAL)
C
Quality of life in cancer patients treated with mistletoe: a systematic review and meta-analysis
C
Cancer Patients' Experiences of Using Mistletoe (Viscum album): A Qualitative Systematic Review and Synthesis
C
Survival of Cancer Patients Treated with Non-Fermented Mistletoe Extract: A Systematic Review and Meta-Analysis
C
Mistletoe as complementary treatment in patients with advanced non-small-cell lung cancer treated with carboplatin-based combinations: a randomised phase II study
C
Integrative medicine during the intensive phase of chemotherapy in pediatric oncology in Germany: a randomized controlled trial with 5-year follow up.
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