Label: ZINC THERAPY- pyrithione zinc liquid
-
NDC Code(s):
71819-007-04,
71819-007-10,
71819-007-12,
71819-007-64, view more71819-007-99
- Packager: D3 Development, Inc.
- Category: HUMAN OTC DRUG LABEL
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.
Drug Label Information
Updated July 2, 2019
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- ASK DOCTOR
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- STORAGE AND HANDLING
- INACTIVE INGREDIENT
- QUESTIONS
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
ZINC THERAPY
pyrithione zinc liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71819-007 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5) PYRITHIONE ZINC 2 g in 100 mL Inactive Ingredients Ingredient Name Strength 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 Code Package Description Marketing Start Date Marketing End Date 1 NDC:71819-007-04 118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 01/23/2018 2 NDC:71819-007-12 355 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 01/23/2018 3 NDC:71819-007-64 1893 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 01/23/2018 4 NDC:71819-007-99 3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 01/23/2018 5 NDC:71819-007-10 296 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/02/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part358H 01/23/2018 Labeler - D3 Development, Inc. (043195877)