FDA.reportPublic FDA data

WATER

Manufacturer
Uriel Pharmacy Inc.
Effective date
2025-11-17
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 02:35:14

Label at a glance#

ProductFormica Stibium comp.
Active ingredientSUS SCROFA LUNG, ANTIMONY, SILICON DIOXIDE, FORMICA RUFA
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: 10 drops. Ages 2-11: 5 drops. Under age 2: Consult a doctor.

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: Pulmo (Bovine lung) 6X, Stibium met. (Antimony) 8X, Nontronite (Nat. Iron silicate) 12X, Formica (Red wood ant) 15X

INACTIVE INGREDIENT SECTION

Inactive Ingredient: Distilled water

Prepared using rhythmical processes.

OTC - PURPOSE SECTION

Use: Temporary relief of cough.

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.

REFRIGERATE AFTER OPENING.
BEST WHEN USED WITHIN 30 DAYS OF OPENING.

OTC - QUESTIONS SECTION

Questions? Call 866.642.2858
Made with care by Uriel, East Troy, WI 53120
shopuriel.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Formica Stibium comp. LiquidFormica Stibium comp. Liquid

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-4200-3Formica Stibium comp.60 mL in 1 BOTTLE, DROPPERLIQUID603

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ANTIMONYACTIVE INGREDIENT9IT35J3UV31
COLLOIDAL SILICON DIOXIDEACTIVE INGREDIENTETJ7Z6XBU41
FORMICA RUFAACTIVE INGREDIENT55H0W83JO51
SUS SCROFA LUNGACTIVE INGREDIENT7GL3G1COB31
ANTIMONYACTIVE MOIETY9IT35J3UV31
COLLOIDAL SILICON DIOXIDEACTIVE MOIETYETJ7Z6XBU41
FORMICA RUFAACTIVE MOIETY55H0W83JO51
SUS SCROFA LUNGACTIVE MOIETY7GL3G1COB31
WATERINACTIVE INGREDIENT059QF0KO0R1

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
48951-420048951-4200-3

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
SUS SCROFA LUNG7GL3G1COB3ACTIB
ANTIMONY9IT35J3UV3ACTIB
SILICON DIOXIDEETJ7Z6XBU4ACTIB
FORMICA RUFA55H0W83JO5ACTIB

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
Formica Stibium comp.FORMICA STIBIUM COMP.Uriel Pharmacy Inc.439073f2-1dee-4b4e-a65e-74aee1c73c2b2025-11-17WarningsExact identifier
ndc (package): 48951-4200-3
ndc (product): 48951-4200
ndc11 (package): 48951420003
spl id: 43d0bb0c-2c3b-8959-e063-6294a90ac75f
spl set id: 439073f2-1dee-4b4e-a65e-74aee1c73c2b

Reported adverse events (FAERS/openFDA)#

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