Viscum Abietis Special Series 2
- Manufacturer
- Uriel Pharmacy Inc.
- Effective date
- 2018-05-14
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- legacy-cache
- Hydrated at
- 2026-08-02 00:58:00
Label at a glance#
ProductViscum Abietis Special Series 2
Active ingredientVISCUM ALBUM FRUITING TOP
Label structure9 sections
Contacts and useful links#
Websitewww.urielpharmacy.com
www.urielpharmacy.com
www.urielpharmacy.comLabel contents#
Full prescribing information#
INDICATIONS & USAGE SECTION
Directions: FOR ORAL USE.
DOSAGE & ADMINISTRATION SECTION
Take the contents of one ampule under the tongue and hold for 30 seconds, then swallow.
OTC - ACTIVE INGREDIENT SECTION
Active Ingredient: Viscum Abietis (Fir tree mistletoe)
4 amps 5mg = 1 gm contains: 2X, 500mg
2 amps 20mg = 1 gm contains: 1X, 200mg
3 amps 30mg = 1 gm contains: 1X, 300mg
INACTIVE INGREDIENT SECTION
Inactive Ingredients: Water, Salt, Sodium hydroxide
OTC - PURPOSE SECTION
Use: Temporary relief of headache.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
KEEP OUT OF REACH OF CHILDREN.
WARNINGS SECTION
Warnings: Claims based on traditional homepathic practice, not accepted medical evidence. Not FDA evaluated. Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions or if conditions worsen or persist. If pregnant or nursing, consult a doctor before use.
OTC - QUESTIONS SECTION
Questions? Call 866.642.2858 Uriel, East Troy, WI 53120
www.urielpharmacy.com
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
Products#
Every source-derived product name is available through these pages.
- Viscum Abietis Special Series 2
- SODIUM HYDROXIDE
- VISCUM ALBUM FRUITING TOP
- WATER
- SODIUM CHLORIDE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 48951-9323 | 48951-9323-1 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| SODIUM HYDROXIDE | 55X04QC32I | IACT |
| VISCUM ALBUM FRUITING TOP | BK9092J5MP | ACTIB |
| WATER | 059QF0KO0R | IACT |
| SODIUM CHLORIDE | 451W47IQ8X | IACT |
Source Document#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| c68bb4c8-6556-448b-e053-2a95a90ada81 | 6c2cbf19-d274-e8e6-e053-2991aa0acadb | 2021-07-07 | Warnings | 6c2cbf19-d274-e8e6-e053-2991aa0acadb |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.