SPL v1
SPL
SPL Set ID 16e5b8b5-6815-43f3-8365-9ab6e5c87044
Route
TOPICAL
Published
Effective Date 2025-09-18
Document Type 34390-5 HUMAN OTC DRUG LABEL

Drug Facts

Composition & Product

Active Ingredients
Salicylic Acid (3 g)
Inactive Ingredients
Propylene Glycol Alcohol Hydroxypropyl Cellulose (1600000 Wamw) Water

Identifiers & Packaging

Marketing Status
UNAPPROVED DRUG OTHER Active Since 2025-09-15
Description

Forreal Pharmaceuticals, LLC - SALICYLIC ACID 3% GEL ACTIVE INGREDIENT SALICYLIC ACID 3%

Medication Information

Warnings and Precautions

WARNINGS

FOR EXTERNAL USE ONLY

ASK A DOCTOR BEFORE USE IF CONDITION COVERS A LARGE AREA OF THE BODY

Indications and Usage

USES

HELPS STOP THESE SYMPTOMS OF PSORIASIS, SEBORRHEIC DERMATITIS AND DANDRUFF

  • FLAKING
  • SCALING
  • REDNESS
  • IRRITATION
  • ITCHING
Dosage and Administration

DIRECTIONS

  • APPLY TO AFFECTED AREA ONE TO FOUR TIMES DAILY OR AS DIRECTED BY A DOCTOR.
Description

Forreal Pharmaceuticals, LLC - SALICYLIC ACID 3% GEL ACTIVE INGREDIENT SALICYLIC ACID 3%

Section 50565-1

KEEP OUT OF REACH OF CHILDREN. IN CASE OF ACCIDENTAL INGESTION, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.

FLAMMABLE

Section 50567-7

WHEN USING THIS PRODUCT

  • DO NOT GET INTO EYES. IF CONTACT OCCURS, RINSE EYES THOROUGHLY WITH WATER. IF IRRITATION PERSISTS, CONSULT A DOCTOR.

STOP USE AND CONSULT A DOCTOR IF CONDITION WORSENS OR DOES NOT IMPROVE AFTER REGULAR USE.

Section 51727-6

INACTIVE INGREDIENTS

PROPYLENE GLYCOL, SD-40 ALCOHOL (21%), WATER, HYDROXYPROPYLCELLULOSE

Section 55105-1

PURPOSE

PSORIASIS, SEBORRHEIC DERMATITIS

Section 55106-9

Forreal Pharmaceuticals, LLC - SALICYLIC ACID 3% GEL

ACTIVE INGREDIENT

SALICYLIC ACID 3%

Principal Display Panel

NDC 81877-727-30

Salicylic Acid 3% Gel

Forreal Pharmaceuticals

YOUR SOLUTION TO BETTER HEALTHCARE.

NET WT 1 OZ (28.4 g)

Structured Label Content

Indications and Usage (34067-9)

USES

HELPS STOP THESE SYMPTOMS OF PSORIASIS, SEBORRHEIC DERMATITIS AND DANDRUFF

  • FLAKING
  • SCALING
  • REDNESS
  • IRRITATION
  • ITCHING
Dosage and Administration (34068-7)

DIRECTIONS

  • APPLY TO AFFECTED AREA ONE TO FOUR TIMES DAILY OR AS DIRECTED BY A DOCTOR.
Warnings and Precautions (34071-1)

WARNINGS

FOR EXTERNAL USE ONLY

ASK A DOCTOR BEFORE USE IF CONDITION COVERS A LARGE AREA OF THE BODY

Section 50565-1 (50565-1)

KEEP OUT OF REACH OF CHILDREN. IN CASE OF ACCIDENTAL INGESTION, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.

FLAMMABLE

Section 50567-7 (50567-7)

WHEN USING THIS PRODUCT

  • DO NOT GET INTO EYES. IF CONTACT OCCURS, RINSE EYES THOROUGHLY WITH WATER. IF IRRITATION PERSISTS, CONSULT A DOCTOR.

STOP USE AND CONSULT A DOCTOR IF CONDITION WORSENS OR DOES NOT IMPROVE AFTER REGULAR USE.

Section 51727-6 (51727-6)

INACTIVE INGREDIENTS

PROPYLENE GLYCOL, SD-40 ALCOHOL (21%), WATER, HYDROXYPROPYLCELLULOSE

Section 55105-1 (55105-1)

PURPOSE

PSORIASIS, SEBORRHEIC DERMATITIS

Section 55106-9 (55106-9)

Forreal Pharmaceuticals, LLC - SALICYLIC ACID 3% GEL

ACTIVE INGREDIENT

SALICYLIC ACID 3%

Principal Display Panel (PRINCIPAL DISPLAY PANEL)

NDC 81877-727-30

Salicylic Acid 3% Gel

Forreal Pharmaceuticals

YOUR SOLUTION TO BETTER HEALTHCARE.

NET WT 1 OZ (28.4 g)

Advanced Ingredient Data

Raw Label Data

All Sections (JSON)

Additional Information

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Source: dailymed · Ingested: 2026-02-15T12:07:04.845532 · Updated: 2026-03-14T23:10:16.319664