FDA.reportPublic FDA data

Apis Phosphorus

Manufacturer
Uriel Pharmacy Inc
Effective date
2021-11-19
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:15:12

Label at a glance#

ProductApis Phosphorus
Active ingredientPHOSPHORUS, APIS MELLIFERA, SILVER SULFIDE
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 Ingredients: Apis (Honeybee) 6X, Dyscrasite (Antimony silver sulfide) 6X, Phosphorus (Yellow phosphorus) 6X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Water, Salt, Lactose

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 worse or persist. Contains traces of lactose. If pregnant or nursing, consult a doctor before use.

OTC - QUESTIONS SECTION

Questions? Call 866.642.2858
Uriel, East Troy, WI 53120
shopuriel.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Apis Phosphorus AmpulesApis Phosphorus Ampules

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6cca4355-1206-91f7-02de-17eef38a8622Product name120140508
751c581a-bf64-2fd7-b3ec-ca02c83e4a00Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-1353-1Apis Phosphorus1 mL in 1 AMPULELIQUID12
48951-1353-1Apis Phosphorus10 in 1 BOXLIQUID102

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-1353APIS PHOSPHORUS LIQUID [URIEL PHARMACY INC]2Legacy NDC, 2 package rows20211212_d2cdb098-468a-3555-e053-2995a90ac7ca.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
48951-135348951-1353-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
LACTOSE, UNSPECIFIED FORMJ2B2A4N98GIACT
PHOSPHORUS27YLU75U4WACTIB
APIS MELLIFERA7S82P3R43ZACTIB
SILVER SULFIDE9ZB10YHC1CACTIB
SODIUM CHLORIDE451W47IQ8XIACT

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
d2d18086-8f38-1acf-e053-2a95a90ac9e3d2cdb098-468a-3555-e053-2995a90ac7ca2021-11-19WarningsExact identifier
spl id: d2d18086-8f38-1acf-e053-2a95a90ac9e3
spl set id: d2cdb098-468a-3555-e053-2995a90ac7ca

Reported adverse events (FAERS/openFDA)#

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