Triderma Baby Stubborn Eczema Itch Relief Cream
FDA Label NDC 10738-069
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Genuine Aloe Virgin Corporation for the product Triderma Baby Stubborn Eczema Itch Relief (NDC 10738-069). 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 drug facts, active ingredient, purpose, packaging, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Colloidal Oatmeal 1.5%
Purpose
Skin Protectant
Packaging
Untitled (Untitled)
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