FDA.reportPublic FDA data

Pulmo Tartarus 6/8 Special Order

Manufacturer
Uriel Pharmacy Inc.
Effective date
2018-05-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:58:50

Label at a glance#

ProductPulmo Tartarus 6/8 Special Order
Active ingredientANTIMONY POTASSIUM TARTRATE, SUS SCROFA LUNG
Label structure9 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Directions: ONLY FOR USE AS A NASAL SPRAY.

DOSAGE & ADMINISTRATION SECTION

Ages 12 and older: 2-3 sprays. Ages 2-11: 1-2 sprays. Under age 2: Consult a doctor.

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: Pulmo (Bovine lung) 6X, Tartarus stibiatus (Potassium antimonotartrate) 8X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Water, Salt, Grapefruit seed extract, Lactose

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. Contains traces of lactose. If pregnant or nursing, consult a doctor before use. Do not use if safety seals on box are broken or missing.
SHAKE WELL BEFORE USE.
REFRIGERATE AFTER OPENING.
USE WITHIN 30 DAYS OF OPENING.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PulmoTartarus68SOSprayPulmoTartarus68SOSpray

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
48951-832348951-8323-2

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
SODIUM CHLORIDE451W47IQ8XIACT
ANTIMONY POTASSIUM TARTRATEDL6OZ476V3ACTIB
CITRUS PARADISI SEED12F08874Y7IACT
LACTOSE, UNSPECIFIED FORMJ2B2A4N98GIACT
SUS SCROFA LUNG7GL3G1COB3ACTIB

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
b5e462f8-565c-e45f-e053-2995a90a5ae26bb3c3b0-2d12-4c40-e053-2a91aa0a04de2020-12-07WarningsExact identifier
spl set id: 6bb3c3b0-2d12-4c40-e053-2a91aa0a04de

Reported adverse events (FAERS/openFDA)#

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