Purpose
Uses: Use according to standard homeopathic indications.
Saline
FDA Label NDC 48951-9998
Full FDA labeling including 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 Saline (NDC 48951-9998). 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 purpose, dosage & administration, otc-active ingredient, inactive ingredient, keep out of reach of children, do not use section, ask doctor section, pregnancy or breast feeding section, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Dosage & Administration
Directions: Take contents of 1 vial once daily.
Otc-Active Ingredient
Active Ingredient: Natrum muriaticum (Sea Salt) 1X HPUS.
Inactive Ingredient
Inactive Ingredient: Water.
Keep Out Of Reach Of Children
KEEP OUT OF REACH OF CHILDREN.
Do Not Use Section
Warnings:
Do not use if allergic to any ingredient.
Ask Doctor Section
For serious conditions, consult a doctor before use.
Pregnancy Or Breast Feeding Section
If you are pregnant or nursing, consult a doctor before use.
Questions Section
Questions? Uriel Pharmacy
866 642-2858 East Troy, WI 53120
www.urielpharmacy.com
NDC 48951-9998-1
Principal Display Panel
Saline 
Homeopathic Vials
net vol. 10 ml (1/3 fl. oz.)
Saline Vials Label (Salv01)
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