FDA.reportPublic FDA data

Pert 2 in 1

Manufacturer
Sodalis USA, LLC
Effective date
2025-08-13
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 01:10:28

Label at a glance#

ProductPert 2 in 1 Advanced plus
Active ingredientSALICYLIC ACID
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Salicylic Acid 2%

OTC - PURPOSE SECTION

Purpose

Antidandruff

INDICATIONS & USAGE SECTION

Use Controls the symptoms of dandruff

WARNINGS SECTION

Warnings

For external use only

OTC - WHEN USING SECTION

When using this product

  • avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if

condition worsens or does not improve after regular use of this product as directed.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Directions

  • For best results, use at least twice a week or as directed by a doctor
  • Shake before use.
  • Gently massage into wet hair and scalp, lather and rinse. Repeat if desired.

INACTIVE INGREDIENT SECTION

Inactive ingredients: Water (Aqua), Sodium Laureth Sulfate, Sodium Lauryl Sulfate, Cocamidopropyl Betaine, Glycerin, Cocamide MEA, Dimethicone, Glycol Distearate, Fragrance (Parfum), Guar Hydroxypropyltrimonium Chloride, Sodium Citrate, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Sodium Benzoate, Sodium Chloride, Methylchloroisothiazolinone, Methylisothiazolinone, Yellow 10 (CI47005), Blue 1 (CI42090).

OTC - QUESTIONS SECTION

Questions or Comments?

1-800-575-7960 www.pert.com

SPL UNCLASSIFIED SECTION

PERT®

2IN1 ADVANCED+

  • 2% Salicylic Acid
  • Helps Control Dandruff
  • Fast-Acting

Distributed by: Sodalis USA, LLC

Westport, CT 06880

Made in Canada.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PERT®

PLUS ODORX™

ODOR ELIMINATING TECHNOLOGY

ORIGINAL STRENGTH

ANTI-DANDRUFF

2 IN 1

with 2% SALICYLIC ACID

QUAD ACTION FORMULA

  • Cleans
  • Conditions
  • Reduces Flakes
  • Fights Odors

Shampoo+Conditioner

24.5 fl oz (750 mL)

1L label1L label

labellabel

drug factsdrug facts

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
205104salicylic acid 2 % Medicated ShampooPSN5
205104salicylic acid 20 MG/ML Medicated ShampooSCD5
205104salicylic acid 2 % Medicated ConditionerSY5
205104salicylic acid 2 % Medicated ShampooSY5

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
f1e0dc7e-7d61-4625-b6d9-4894927679d7Product name220211025
e4870509-7e28-6f92-f0be-dd3dd889a9cfProduct name520200810
6e9d4a47-c464-b93e-aebc-ad7bffc9c4cdProduct name220190619
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316
5668b646-cd56-c3c7-bdea-3f6b1a8840dbProduct name120140508
684ea482-2e8b-14af-5664-b98f1e402036Product name120140508
810ab97e-f109-f41c-7c83-6a652a9cbf43Product name120140508
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
8dbefedf-0a0d-a224-5a3c-66dc9e11c2ddProduct name120140508
b060cc1a-fe47-856b-0b77-4448b5963de8Product name120140508
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81277-802-13Pert 2 in 1Advanced plus400 mL in 1 BOTTLESHAMPOO4005
81277-802-25Pert 2 in 1Advanced plus750 mL in 1 BOTTLESHAMPOO7505
81277-802-33Pert 2 in 1Advanced plus1000 mL in 1 BOTTLESHAMPOO10005

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81277-80281277-802-13, 81277-802-25, 81277-802-33

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Name, UNII, Kind table
NameUNIIKind
SALICYLIC ACIDO414PZ4LPZACTIB
GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE)B16G315W7AIACT
ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S)8Z5ZAL5H3VIACT
GLYCERINPDC6A3C0OXIACT
COCO MONOETHANOLAMIDEC80684146DIACT
GLYCOL DISTEARATE13W7MDN21WIACT
SODIUM CITRATE1Q73Q2JULRIACT
WATER059QF0KO0RIACT
DIMETHICONE92RU3N3Y1OIACT
SODIUM BENZOATEOJ245FE5EUIACT
SODIUM CHLORIDE451W47IQ8XIACT
D&C YELLOW NO. 1035SW5USQ3GIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
SODIUM LAURETH SULFATEBPV390UAP0IACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT
SODIUM LAURYL SULFATE368GB5141JIACT
METHYLCHLOROISOTHIAZOLINONEDEL7T5QRPNIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Pert 2 in 1 Advanced plusSALICYLIC ACIDSodalis USA, LLC0eaed46c-ae6f-0d58-e063-6394a90ad2a32025-08-13WarningsExact identifier
ndc (package): 81277-802-33
ndc (package): 81277-802-13
ndc (package): 81277-802-25
ndc (product): 81277-802
ndc11 (package): 81277080233
ndc11 (package): 81277080213
ndc11 (package): 81277080225
spl id: 3c57af2e-d2ed-9ac1-e063-6294a90a6c32
spl set id: 0eaed46c-ae6f-0d58-e063-6394a90ad2a3

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.