CONTROL DANDRUFF THERAPY- dandruff therapy shampoo shampoo 
Kamedis

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Control - Dandruff Therapy Shampoo

Drug Facts

Active ingredient

Pyrithione Zinc 1.0%

Purpose

Anti-Dandruff

Use

  • helps eliminate flaking, itching and scaling associated with dandruff and seborrheic dermatitis

Warnings

For external use only

When using this product

  • avoid contact with the 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.
  • If condition covers a large area of the body, consult your doctor before using this product.

Directions

  • adults and children 3 years of age and older: 
  •    apply to wet hair 
  •    gently massage into hair and scalp and leave for 2-3 minutes before thoroughly rinsing 
  •    rinse and repeat if desired 
  •    for best results use at least twice a week or as directed by your doctor

Inactive ingredients

ammonium laureth sulfate, water, ammonium lauryl sulfate, cocamidopropyl betaine, sodium lauroyl sarcosinate, soapberry (Sapindus mukurossi) fruit extract, salicylic acid, salt (sodium chloride), polyquaternium-10, sodium benzoate, triethanolamine, fragrance

Made in USA
(US and non US ingredients) Manufactured for
Kamedis Pennsylvania, 18109.

www.kamedis.com

PRINCIPAL DISPLAY PANEL - 200 mL Bottle Carton

Kamedis®
Skin Restoring Solutions

BOTANIPLEX
TECHNOLOGY

SCALP
CONTROL
Dandruff Therapy
Shampoo

PYRITHIONE ZINC 1%

Clinically proven to remove up to
100% visible dandruff. Helps eliminate
flaking, scaling, itching, irritation and
redness associated with dandruff

DERMATOLOGIST
RECOMMENDED

Free from Parabens, Steroids,
Dyes, Sodium Lauryl Sulfate, Tar

200 mL
6.7 fl oz

PRINCIPAL DISPLAY PANEL -  200 mL Bottle Carton
CONTROL DANDRUFF THERAPY 
dandruff therapy shampoo shampoo
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50718-0021
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5) PYRITHIONE ZINC10 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)  
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
SALICYLIC ACID (UNII: O414PZ4LPZ)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SAPINDUS MUKOROSSI FRUIT (UNII: 66H9NW427Y)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SODIUM LAUROYL SARCOSINATE (UNII: 632GS99618)  
WATER (UNII: 059QF0KO0R)  
TROLAMINE (UNII: 9O3K93S3TK)  
AMMONIUM LAURETH-2 SULFATE (UNII: 698O4Z48G6)  
POLYQUATERNIUM-10 (10000 MPA.S AT 2%) (UNII: PI1STR9QYH)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:50718-0021-11 in 1 CARTON01/01/2018
1200 mL in 1 BOTTLE; Type 0: Not a Combination Product
2NDC:50718-0021-2500 mL in 1 BOTTLE; Type 0: Not a Combination Product01/01/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph drugM03201/01/2018
Labeler - Kamedis (080311300)

Revised: 12/2023
Document Id: 6820d2bc-1aaf-4bca-ae9a-d1509d8f4232
Set id: 2a5fc8ae-1d98-496c-a6ca-922897e3ab47
Version: 5
Effective Time: 20231218
 
Kamedis