SALICYCLIC ACID 3% GEL- salicyclic acid 3% gel

Salicyclic Acid 3% Gel by

Drug Labeling and Warnings

Salicyclic Acid 3% Gel by is a Otc medication manufactured, distributed, or labeled by FORREAL PHARMACEUTICALS LLC . Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Forreal Pharmaceuticals, LLC - SALICYLIC ACID 3% GEL

ACTIVE INGREDIENT

SALICYLIC ACID 3%

PURPOSE

PURPOSE

PSORIASIS, SEBORRHEIC DERMATITIS

INDICATIONS & USAGE

USES

HELPS STOP THESE SYMPTOMS OF PSORIASIS, SEBORRHEIC DERMATITIS AND DANDRUFF

• FLAKING
• SCALING
• REDNESS
• IRRITATION
• ITCHING

WARNINGS

WARNINGS

FOR EXTERNAL USE ONLY

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

WHEN USING

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.

KEEP OUT OF REACH OF CHILDREN

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

FLAMMABLE

DOSAGE & ADMINISTRATION

DIRECTIONS

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

INACTIVE INGREDIENT

INACTIVE INGREDIENTS

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

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)

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)

INGREDIENTS AND APPEARANCE

SALICYCLIC ACID 3% GEL 
salicyclic acid 3% gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81877-727
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	3 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ALCOHOL (UNII: 3K9958V90M)
HYDROXYPROPYL CELLULOSE (1600000 WAMW) (UNII: RFW2ET671P)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81877-727-30	28.4 g in 1 TUBE; Type 0: Not a Combination Product	09/15/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Unapproved drug other		09/15/2025

Labeler - FORREAL PHARMACEUTICALS LLC (118029197)