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OTC products · Product label record

The Acne Spot Treatment drug information

SALICYLIC ACID SPOT
Spotless, Inc. · TOPICAL

Product NDC: 87415-100

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Source label information, not individualized medical advice. This record applies to the product and labeler shown below. Compare the exact formulation, strength and country with your package and the current source label.
Generic nameSALICYLIC ACID SPOT
Labeler / manufacturerSpotless, Inc.
RouteTOPICAL
Drug classDrug class not supplied in source label
Product NDC87415-100
Label effective date2026-08-30

Official product label reference

The Acne Spot Treatment — Spotless, Inc.

This page contains 9 source sections for SALICYLIC ACID SPOT, topical route. Label set 4a1a3716-9eaf-6be4-e063-6294a90a31c3, version 2.

Retrieved 2026-10-02 · openFDA dataset updated 2026-10-02 · Check the current DailyMed label

Label records can cover multiple strengths or package sizes. A label listing does not by itself establish FDA approval or current market availability. Check the source and application history for this specific product.

Uses described in the label

Uses • for treatment of acne

Purpose

Purpose Acne Medication
Dosage and administration — label text
Drug Facts Drug Facts
Warnings
Warnings For external use only Flammable, keep away from open fire or flame When using this product skin irritation and dryness is more likely to occur if you use another topical medication at the same time. If irritation occurs, only use one topical acne medication at a time. Keep out of reach of children. If swallowed, get medical help or contact Poison Control Center right away. Avoid contact with eyes. If contact occurs, flush thoroughly with water.
Active ingredient
Active ingredients Salicylic Acid 2%
While using this medicine
When using this product skin irritation and dryness is more likely to occur if you use another topical medication at the same time. If irritation occurs, only use one topical acne medication at a time.
Child safety
Keep out of reach of children. If swallowed, get medical help or contact Poison Control Center right away. Avoid contact with eyes. If contact occurs, flush thoroughly with water.
Instructions for use
Directions • Clean the skin thoroughly before applying this product. • Cover the entire affected area with a thin layer one to three times daily • Because excessive drying of the skin may occur, start with one application daily, then gradually increase to two times daily if needed or as directed by a doctor • If bothersome dryness or peeling occurs, reduce application to once a day or every other day • Always wear sunscreen after daytime use
Inactive ingredient
Inactive ingredients Water, Niacinamide, Glycerin, Pentylene Glycol, Sodium Polyacrylate, Polyacrylate Crosspolymer-6, Epigallocatechin Gallatyl Glucoside, Epigallocatechin Gallate, Madecassoside, Zinc PCA, Sphingomonas Ferment Extract, Panthenol, Sodium Polyacryloyldimethyl Taurate, Caprylyl Glycol, Ethylhexylglycerin, Tocopherol

Official sources and product identifiers

Substances listed: SALICYLIC ACID

RxNorm identifiers: 346298

Package NDC codes

87415-100-04

Further research and background

These are external searches for related information. Research, encyclopedia and news articles have not been imported into this product record.

Coverage and corrections

The text is extracted from a US structured product label. Tables are represented as text where supplied; formatting and illustrations may be lost. A missing section does not mean a risk is absent. This reference has not been independently reviewed by a clinician and is not a live safety-alert service.

Source retrieved 2026-10-02. Read the source policy.