Tamper Evident: Do Not Use If Imrinted Safety Seal Under Cap Is Broken Or Missingdrug Facts
Active Ingredient (in each tablet)
Sodium Chloride, USP 1.0 gram
Sodium Chloride Tablet
FDA Label NDC 57237-361
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Rising Pharma Holdings, Inc. for the product Sodium Chloride (NDC 57237-361). 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 tamper evident: do not use if imrinted safety seal under cap is broken or missingdrug facts, purpose, other ingredients, other, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Electrolyte Replenisher
Other Ingredients
None
Other
Distributed by:
Rising Pharma Holdings, Inc.
East Brunswick, NJ 08816
Issued: 10/2025
Package Label.Principal Display Panel
Sodium Chloride Tablets, USP
1 Gram
- Normal salt tablets
- For solution or oral use
100 Tablets
Sodium-chloride-label (Sodium Chloride Label) 
* Please review the disclaimer below.
