FDA.reportPublic FDA data

Apis Eucalyptus Special Order

Manufacturer
Uriel Pharmacy Inc.
Effective date
2018-12-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:43:30

Label at a glance#

ProductApis Eucalyptus Special Order
Active ingredientAPIS MELLIFERA, EUCALYPTUS GUM, ATROPA BELLADONNA
Label structure9 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Directions: FOR ORAL USE ONLY.

DOSAGE & ADMINISTRATION SECTION

Take 3-4 times daily. Ages 12 and older: 1/8 teaspoon. Ages 2-11: 1/16 teaspoon. Under age 2: Consult a doctor.

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: Apis (Honeybee) 3X, Atropa belladonna (Nightshade) 3X, Eucalyptus 3X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Kaolin, Distilled water

OTC - PURPOSE SECTION

Use: Temporary relief of sore throat.

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. Do not use if safety seal is broken or missing.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Apis Eucalyptus Special Order PowderApis Eucalyptus Special Order Powder

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
48951-131248951-1312-4

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
APIS MELLIFERA7S82P3R43ZACTIB
EUCALYPTUS GUM72T9EZC2VXACTIB
KAOLIN24H4NWX5COIACT
WATER059QF0KO0RIACT
ATROPA BELLADONNAWQZ3G9PF0HACTIB

Source Document#

Source XML · Source PDF

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
ed9b00de-1e0b-4821-e053-2a95a90a9a827cc59c35-30b6-c964-e053-2a91aa0a09442022-11-16WarningsExact identifier
spl set id: 7cc59c35-30b6-c964-e053-2a91aa0a0944

Reported adverse events (FAERS/openFDA)#

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