PERT 2 IN 1 EXTRA STRENGTH- salicylic acid shampoo

Pert 2 in 1 by

Drug Labeling and Warnings

Pert 2 in 1 by is a Otc medication manufactured, distributed, or labeled by Sodalis USA, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

ACTIVE INGREDIENT

Active ingredient

Salicylic Acid 3%

PURPOSE

Purpose

Antidandruff

INDICATIONS & USAGE

Use Controls the symptoms of dandruff

WARNINGS

Warnings

For external use only

When using this product

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

Stop use and ask a doctor if

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

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

DOSAGE & ADMINISTRATION

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

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, sodium hydroxide, D-limonene, linalool, FD&C Yellow no. 10, FD&C Blue no. 1

QUESTIONS

Questions or Comments?

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

SPL UNCLASSIFIED SECTION

Distributed by: Sodalis USA, LLC.

Westport, CT 06880

Pert is a registered trademark of Sodalis USA, LLC.

Made in Canada

PRINCIPAL DISPLAY PANEL

PERT ®

2 IN 1

ADVANCED+

EXTRA STRENGTH

ANTI-DANDRUFF

• With 3% Salicylic Acid
• Tough on dandruff, gentle on skin
• Helps control flakes caused by dandruff
• Free of parabens and phthalates

SHAMPOO+CONDITIONER+SALICYLIC ACID

12 FL OZ (355 mL)

INGREDIENTS AND APPEARANCE

PERT 2 IN 1  EXTRA STRENGTH
salicylic acid shampoo

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81277-803
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 mL

Inactive Ingredients
Ingredient Name	Strength
LINALOOL (UNII: D81QY6I88E)
LIMONENE, (+)- (UNII: GFD7C86Q1W)
GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE) (UNII: B16G315W7A)
ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V)
GLYCERIN (UNII: PDC6A3C0OX)
COCO MONOETHANOLAMIDE (UNII: C80684146D)
GLYCOL DISTEARATE (UNII: 13W7MDN21W)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
WATER (UNII: 059QF0KO0R)
DIMETHICONE (UNII: 92RU3N3Y1O)
SODIUM BENZOATE (UNII: OJ245FE5EU)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81277-803-12	355 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/18/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M032	11/18/2024

Labeler - Sodalis USA, LLC (119375257)