Active Ingredient
Salicylic Acid
Liquid
FDA Label NDC 61354-091
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Oxygen Development Llc for the product Liquid (NDC 61354-091). 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 active ingredient, purpose, uses, warnings, when using this product, keep out of reach of children, directions, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Acne Treatment
Uses
For the treatment of acne
Helps prevent new acne blemishes from forming
Warnings
For external use only
When Using This Product
Skin irritation and dryness are more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne treatment at a time.
Avoid contact with eyes. If products occurs, rinse eyes thoroughly with water
Keep Out Of Reach Of Children
If product is swallowed, get medical help or contact a poison control center immediately
Directions
Shake well before use
Start with damp skin
Apply a small amount onto your fingertips and emulsify
Gently cleanse the skin using circular motions
Rinse with warm water and gently pat the skin dry
Follow with your MONAT Skincare Routine
Inactive Ingredients
Water/Aqua, Sodium Cocoyl Glutamate, Sodium Cocoyl Isethionate, Propanediol, Sodium C14-16 Olefin Sulfonate, Cocamidopropyl Betaine, Niacinamide, Cocamide MIPA, Glycerin, PEG-150 Distearate, Stearic Acid, Coconut Acid, Sodium PCA, Maclura Cochinchinensis Leaf Prenylflavonoids, Glycol Distearate, Laureth-4, PEG-120 Methyl Glucose Dioleate, Caprylyl/Capryl Glucoside, Polyglyceryl-10 Laurate, Polyglyceryl-10 Oleate, Sodium Chloride, SOdium Benzoate, Potassium Sorbate
Package Label
61354-091-01_aw (22 6416)
61354-091-01_aw (P2779)
* Please review the disclaimer below.
