ZINC THERAPY- pyrithione zinc soap 
D3 Development, Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Zinc Therapy Soap Bar

Drug Facts

Active ingredient

Pyrithione zinc 2%

Purpose

Dandruff, Seborrheic dermatitis

Uses

Controls and reduces the symptoms of dandruff and seborrheic dermatitis.

Warnings

For external use only

Ask a doctor before use if you have a condition that covers a large area of the body.

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 as directed.

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

Directions

  • Use on affected areas in place of your regular soap
  • For best results use at least twice a week or as directed by a doctor
  • Work up a lather using warm water and massage into affected areas
  • Rinse well

Other information

  • Store at room temperature
  • Lot number and expiration date are printed on back panel.

Inactive ingredients

Sodium palmate, sodium cocoate*, sodium palm kernelate*, water, glycerin, titanium dioxide, Avena Sativa (oat) kernel flour, olive oil, vitamin E, table salt, pentasodium pentetate

Questions?

1-800-827-3730

www.dermaharmony.com

Distributed by:

D3 Development, Inc., Portland, ME 04101

Made in the USA

dermaharmony

Zinc Therapy SOAP

2% Pyrithione Zinc for Seborrheic Dermatitis & Dandruff

NET WT 4.0 OZ (113 G)

Zinc Therapy Bar Final

ZINC THERAPY 
pyrithione zinc soap
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71819-001
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5) PYRITHIONE ZINC2 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
WATER (UNII: 059QF0KO0R)  
SODIUM COCOATE (UNII: R1TQH25F4I)  
GLYCERIN (UNII: PDC6A3C0OX)  
OATMEAL (UNII: 8PI54V663Y)  
SODIUM PALM KERNELATE (UNII: 6H91L1NXTW)  
OLIVE OIL (UNII: 6UYK2W1W1E)  
SODIUM PALMATE (UNII: S0A6004K3Z)  
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)  
PENTASODIUM PENTETATE (UNII: 961TOZ5L7T)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71819-001-0128 g in 1 CELLO PACK; Type 0: Not a Combination Product05/01/2018
2NDC:71819-001-04113 g in 1 CELLO PACK; Type 0: Not a Combination Product05/01/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart358H05/01/2018
Labeler - D3 Development, Inc. (043195877)

Revised: 5/2018
 
D3 Development, Inc.