Indications & Usage
FOR ORAL USE ONLY
Pulmo Tartarus 6/8 Liquid
FDA Label NDC 48951-8092
9 label sections · Submitted to the FDA by Uriel Pharmacy Inc. · Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Uriel Pharmacy Inc. for the product Pulmo Tartarus 6/8 (NDC 48951-8092). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding indications & usage, dosage & administration, otc - active ingredient, inactive ingredient, otc - purpose, otc - keep out of reach of children, warnings, otc - questions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Dosage & Administration
Directions: Take the contents of one ampule under the tongue and hold for 30 seconds, then swallow. Follow inside instructions to open ampule.
Otc - Active Ingredient
Active Ingredients: Pulmo (Bovine lung) 6X, Tartarus stibiatus (Potassium antimonotartrate) 8X
Inactive Ingredient
Inactive Ingredients: Water, Salt, Lactose
"prepared using rhythmical processes"
Otc - Purpose
Use: Temporary relief of cough.
Otc - Keep Out Of Reach Of Children
KEEP OUT OF REACH OF CHILDREN.
Warnings
Warnings:
NOT FOR INJECTION
Do not use if allergic to any ingredient. Contains traces of lactose. Consult a physician if symptoms worsen. If pregnant or nursing, consult a physician before use.
Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
Otc - Questions
Questions? Call 866.642.2858 Made by Uriel, East Troy, WI 53120 shopuriel.com
Package Label.Principal Display Panel
Pulmo Tartarus 6/8
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