Itch Relif
FDA Label NDC 69842-038

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Cvs for the product Itch Relif (NDC 69842-038). 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 inactive ingredients:, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Inactive Ingredients:


Camphor
Citric Acid
Diazolidinyl Urea
Glycerin
Hydroxypropyl Methylcellulose
Methylparaben
Propylene Glycol
Propylparaben
SD Alcohol 38-B
Sodium Citrate
Water

* Please review the disclaimer below.