Doo Gro Anti-Dandruff Cream Vitalizer

Manufacturer
J. Strickland & Co. DBA Nature's Protein, Inc. | J. Strickland & Co.
Effective date
2023-10-31
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 23:58:47

Label at a glance#

ProductDoo Gro Anti-Dandruff Vitalizer
Active ingredientPYRITHIONE ZINC
Label structure6 sections

Dosage and administration

Apply to the affected area 1-4 times daily or as directed by a doctor.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Pyrithione Zinc, 0.1%

Purpose

OTC - PURPOSE SECTION

Anti-dandruff

Use:

INDICATIONS & USAGE SECTION

Controls Scalp itching and flaking due to dandruff

Warnings:

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

  • do not get into eyes. If contact occurs, rinse eyes thoroughly with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • condition worsens or does not improve with regular use

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

  • if swallowed, get medical help or call a poison control center at once.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Apply to the affected area 1-4 times daily or as directed by a doctor.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Mineral Oil, Petrolatum, Glycerin, Behentrimonium Methosulfate, Dimethicone, Stearyl Alcohol, Cetyl alcohol, Theobroma Grandiflorum Seed Butter, Oleth-20, Butylene Glycol, Saccharum Officinarum (Sugar Cane) Extract, Citrus Medica Limonum (Lemon) Fruit Extract, Betaine, Hexylene Glycol, Pyrus Malus (Apple) Fruit Extract, Camellia Sinensis Leaf Extract, Hexapeptide-11, Stearyl Dhydroxypropyldimonium Oligosaccharides, Allantoin, Silk Amino Acids, Panthenol, Menthyl Lactate, PPG-26-Buteth-26, PEG-40 Hydrogenated Castor Oil, Sorbitan Trioleate, Propylene Glycol, Diazolidinyl Urea, Methylparaben, Propylparaben, Sodium Sulfate, Fragrance.

Package Labeling

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

12022-005-0012022-005-00

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
247812zinc pyrithione 0.1 % Topical CreamPSN4
247812zinc pyrithione 1 MG/ML Topical CreamSCD4
247812zinc pyrithione 0.1 % Topical CreamSY4

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
d1c9d1af-bddd-448d-86f7-69052b7d5b47Product name120220627

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
12022-005-00Doo Gro Anti-Dandruff Vitalizer100 mL in 1 JARCREAM1004

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
12022-005DOO GRO ANTI-DANDRUFF VITALIZER (PYRITHIONE ZINC) CREAM [J. STRICKLAND & CO. DBA NATURE'S PROTEIN, INC.]4Current NDC, Legacy NDC, 1 package rows20231104_7366c6f8-4cc2-520e-e053-2991aa0a2cc8.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 32 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
12022-00512022-005-00

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 31 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Doo Gro Anti-Dandruff VitalizerPYRITHIONE ZINCJ. Strickland & Co. DBA Nature's Protein, Inc.7366c6f8-4cc2-520e-e053-2991aa0a2cc82023-10-31WarningsExact identifier
ndc (package): 12022-005-00
ndc (product): 12022-005
ndc11 (package): 12022000500
spl id: 0909e89d-1f77-c20a-e063-6294a90a0b46
spl set id: 7366c6f8-4cc2-520e-e053-2991aa0a2cc8

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.