Otc - Active Ingredient
Active Ingredients
Salicylic Acid 1%
Natria
FDA Label NDC 44717-535
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Wasatch Product Development, Inc. for the product Natria (NDC 44717-535). 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 otc - active ingredient, warnings, indications & usage, inactive ingredient, 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
Warnings
Warning: For external use only. Avoid contact with eyes. Rinse with water if eye contact occurs. Discontinue use and contact a doctor if irritation develops and persists.
Indications & Usage
Application: Apply a thin layer evenly over face until completely absorbed. Follow with moisturizer as needed. Use morning and evening.
Inactive Ingredient
Inactive Ingredients: Water (Aqua), Butylene Glycol, Antemisia Princeps extract, algae extract, alpha-glucan oligosaccharide, Glycyrrhiza glabra (licorice) root extract, Retinyl Palmitate (Vitamine A), Panthenyl Triacetate (Vitamin B), Tetrahexyldecyl Ascorbate (Vitamin C), Tocopheryl Acetate (Vitamin E), Aloe Barbadensis, Camellia Oleifera (Green tea) leaf extract, Chamomilla recutita (matricaria) flower extract, Ginkgo biloba leaf extract, panax ginseng root extract, ulva lactuca (sea lettuce) extract, Vitis vinifera (grape) seed extract, ergothioneine, sclerotium gum, PEG-8 dimethicone, Phenoxyethanol, Methylparaben, Butylparaben, Ethylparaben, Propylparaben.
Package Label.Principal Display Panel
Natria
Acne Treatment Gel
30 ml/ 1 fl. oz.
Image Of Primary Label (Primary)
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