KERALYT 3 PERCENT- salicylic acid gel 
Summers Laboratories Inc

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SUMMERS LABS (as PLD) - KERALYT GEL 3% SALICYLIC ACID (11086-038)

ACTIVE INGREDIENT

SALICYLIC ACID 3%

PURPOSE

PSORIASIS, SEBORRHEIC DERMATITIS

USES

HELPS STOP THESE SYMPTOMS OF PSORIASIS, SEBORRHEIC DERMATITIS AND DANDRUFF

WARNINGS

FOR EXTERNAL USE ONLY

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

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

FLAMMABLE

DIRECTIONS

INACTIVE INGREDIENTS

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

Keralyt 3-SA_Unit Carton

KERALYT  3 PERCENT
salicylic acid gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11086-038
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID3 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
ALCOHOL (UNII: 3K9958V90M)  
HYDROXYPROPYL CELLULOSE (UNII: RFW2ET671P)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11086-038-0128.4 g in 1 TUBE; Type 0: Not a Combination Product10/30/2013
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM03210/30/2013
Labeler - Summers Laboratories Inc (002382612)

Revised: 10/2023
Document Id: 074d1247-a817-29b6-e063-6294a90aa64e
Set id: c02018de-3b03-49b7-9152-c65b248345ad
Version: 7
Effective Time: 20231009
 
Summers Laboratories Inc