ZINC THERAPY- pyrithione zinc liquid 
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

Drug Facts

Active ingredient

Pyrithione zinc 2%

Purposes

Dandruff, Seborrheic dermatitis

Uses

Controls, reduces, and helps stop the symptoms of dandruff and seborrheic dermatitis.

Warnings

For external use only

Ask a doctor before use if you have seborrheic dermatitis that covers a large portion 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

Other information

Inactive ingredients

Water, potassium cocoate, potassium oleate, olive oil, vegetable glycerin, coco glucoside, salt, oatmeal, citric acid

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 & Anti-Dandruff

MEDICATED NATURAL CASTILE SOAP

4 FL OZ (118 ml)

DH ZNP 2-2-18

ZINC THERAPY 
pyrithione zinc liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71819-007
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5) PYRITHIONE ZINC2 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
WATER (UNII: 059QF0KO0R)  
POTASSIUM COCOATE (UNII: F8U72V8ZXP)  
GLYCERIN (UNII: PDC6A3C0OX)  
OATMEAL (UNII: 8PI54V663Y)  
POTASSIUM OLEATE (UNII: 74WHF607EU)  
OLIVE OIL (UNII: 6UYK2W1W1E)  
COCO GLUCOSIDE (UNII: ICS790225B)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71819-007-04118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/23/2018
2NDC:71819-007-12355 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/23/2018
3NDC:71819-007-641893 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/23/2018
4NDC:71819-007-993785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/23/2018
5NDC:71819-007-10296 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/02/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart358H01/23/2018
Labeler - D3 Development, Inc. (043195877)

Revised: 7/2019
Document Id: 8cb1d88d-346d-7cf6-e053-2995a90a1d9a
Set id: 637851c6-ff4a-8bbc-e053-2991aa0a963c
Version: 3
Effective Time: 20190702
 
D3 Development, Inc.