Otc - Active Ingredient
Salicylic acid 1% ...........Acne Treatment
Scantily Pad Liquid
FDA Label NDC 81953-100
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Dermala Inc for the product Scantily Pad (NDC 81953-100). 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, otc - purpose, warnings, indications & usage, inactive ingredient, dosage & administration, otc - keep out of reach of children, 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
Otc - Purpose
For the treatment of ACNE
Warnings
WARNINGS For external use only. Skin
irritation and dryness is more likely to
occur when using this product if you use
another topical acne medication at the
same time. If irritation occurs, only use
one topical acne medication at a time.
Indications & Usage
For the treatment of Acne
Inactive Ingredient
INACTIVE INGREDIENTS Organic Aloe vera, organic
grain alcohol, cocamidopropyl dimethylamine, SE
Microbiome ComplexTM, sodium hydroxide, organic
lemon essential oil.
Dosage & Administration
DIRECTIONS Cleanse the skin. Use one pad to apply a
thin layer of solution to affected areas. Start with one
application daily, then increase to two times per day
(morning and evening). If dryness or peeling occurs,
reduce application to once a day or every other day.
Test on a small area of skin before applying to face. If
eye contact occurs, flush thoroughly with water.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children
* Please review the disclaimer below.
