FDA.reportPublic FDA data

Ananassa Resina

Manufacturer
Uriel Pharmacy Inc.
Effective date
2019-11-06
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:11:33

Label at a glance#

ProductAnanassa Resina
Active ingredientPINEAPPLE, SILICON DIOXIDE, LARIX DECIDUA RESIN
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: Ananassa (Pineapple) 30X, Chrysolith (Silicate of magnesium and iron) 30X, Resina laricis (Larch resin) 30X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Water, Salt

OTC - PURPOSE SECTION

Use: Temporary relief of dry skin around the eyes.

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.

OTC - QUESTIONS SECTION

Questions? Call 866.642.2858
Made by Uriel, East Troy, WI 53120
www.urielpharmacy.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Ananassa Resina AmpuleAnanassa Resina Ampule

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
48951-1330-12025-01-30C16284748780-12cef2736-5c92-d83d-e063-dadaa90ab31fAnanassa Resina

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-1330-1Ananassa Resina1 mL in 1 AMPULELIQUID12
48951-1330-1Ananassa Resina10 in 1 BOXLIQUID102

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-1330ANANASSA RESINA LIQUID [URIEL PHARMACY INC.]2Legacy NDC, 2 package rows20191108_96b1cd9e-009d-a000-e053-2a95a90a9b43.zip

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
48951-133048951-1330-1

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
WATER059QF0KO0RIACT
SODIUM CHLORIDE451W47IQ8XIACT
PINEAPPLE2A88ZO081OACTIB
SILICON DIOXIDEETJ7Z6XBU4ACTIB
LARIX DECIDUA RESINAD8LJ73GQFACTIB

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
96b1e2b2-9e71-3489-e053-2995a90a0eb896b1cd9e-009d-a000-e053-2a95a90a9b432019-11-06WarningsExact identifier
spl id: 96b1e2b2-9e71-3489-e053-2995a90a0eb8
spl set id: 96b1cd9e-009d-a000-e053-2a95a90a9b43

Reported adverse events (FAERS/openFDA)#

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