Viscum Pini Special Series 4 7ml

Manufacturer
Uriel Pharmacy Inc.
Effective date
2018-05-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:09:46

Label at a glance#

ProductViscum Pini Special Series 4 7ml
Active ingredientVISCUM ALBUM FRUITING TOP
Label structure9 sections

Label 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 Pini (Pine tree mistletoe)
2 amps 10mg = 2X

2 amps 30mg = 1 gm contains: 1X, 300mg

3 amps 50mg = 1 gm contains: 1X, 500mg

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 homeopathic 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.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ViscumPiniHSpecialSeries4AmpulesViscumPiniHSpecialSeries4Ampules

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-9339-1Viscum Pini Special Series 4 7ml7 in 1 PACKAGE, COMBINATIONLIQUID71
48951-9339-1Viscum Pini Special Series 4 7ml1 mL in 1 AMPULELIQUID11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-9339VISCUM PINI SPECIAL SERIES 4 7ML LIQUID [URIEL PHARMACY INC.]1Legacy NDC, 2 package rows20180517_6c67a057-57bc-268d-e053-2a91aa0afce8.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
48951-933948951-9339-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Source Document#

Source XML

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.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
6c67a057-57bd-268d-e053-2a91aa0afce86c67a057-57bc-268d-e053-2a91aa0afce82018-05-17WarningsExact identifier
spl id: 6c67a057-57bd-268d-e053-2a91aa0afce8
spl set id: 6c67a057-57bc-268d-e053-2a91aa0afce8

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.