FDA.reportPublic FDA data

Hair - Moraz Medical Herbs (1989) Limited

Manufacturer
Moraz Medical Herbs (1989) Limited
Effective date
2017-06-21
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:15:30

Label at a glance#

ProductHair
Active ingredientPYRITHIONE ZINC
Label structure8 sections

Indications and uses

Reduces the symptoms of Dandruff

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Zinc Pyrithione 1%

Purpose

OTC - PURPOSE SECTION

Anti-dandruff

Uses

INDICATIONS & USAGE SECTION

  • Reduces the symptoms of Dandruff

Warning

WARNINGS SECTION

For external use only.

When using this product

OTC - WHEN USING SECTION

  • Keep away from eyes. When in contact with eyes, rinse immediately with water

Stop use and ask a doctor

OTC - STOP USE SECTION

  • if condition worsens or does not improve after regular use as directed

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

  • If swallowed, get medical help or contact a poison control center right away.

Inactive ingredients

DOSAGE & ADMINISTRATION SECTION

  • Lather into hair,leave for 3 minutes, then rinse thoroughly.
  • For best result use at least twice a week or as directed by a doctor.

Inactive ingredients

INACTIVE INGREDIENT SECTION


Rosmarinus Officinalis(Rosemary) Leaf Extract, Ammonium Laureth Sulfate, Ammonium Lauryl Sulfate, Ammonium Chloride, Sodium Laureth Sulfate, Glycol Distearate, Cocamide MEA, PEG-150 Distearate, Polyquaternium-10, Triethanolamine, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Parfum, Hexyl Cinnamal, Linalool, Benzyl Salicylate, Coumarin, Butylphenyl Methylpropional, Citronellol, Aqua, Methylchloroisothiszolinone and Methylisothiazolinone.


Questions or Comments?

OTC - QUESTIONS SECTION


Call +1(914)8108625 Monday through Friday


Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 71159-002-25

moraz galilee medical herbs

HAIR

Herbal Anti-Dandruff Shampoo

Shampooing

Anti Pelliculaire

8.5fl oz. 250 ml

LabelLabel

Products#

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

DailyMed product names page 1 of 1 · 21 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71159-00271159-002-25

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 19 matching rows.

Name, UNII, Kind table
NameUNIIKind
PYRITHIONE ZINCR953O2RHZ5ACTIB
ROSEMARYIJ67X351P9IACT
AMMONIUM LAURYL SULFATEQ7AO2R1M0BIACT
AMMONIUM CHLORIDE01Q9PC255DIACT
SODIUM LAURETH-3 SULFATEBPV390UAP0IACT
GLYCOL DISTEARATE13W7MDN21WIACT
COCO MONOETHANOLAMIDEC80684146DIACT
PEG-150 DISTEARATE6F36Q0I0ACIACT
TROLAMINE9O3K93S3TKIACT
.ALPHA.-HEXYLCINNAMALDEHYDE7X6O37OK2IIACT
LINALOOL, (+/-)-D81QY6I88EIACT
BENZYL SALICYLATEWAO5MNK9TUIACT
COUMARINA4VZ22K1WTIACT
BUTYLPHENYL METHYLPROPIONALT7540GJV69IACT
.BETA.-CITRONELLOL, (R)-P01OUT964KIACT
WATER059QF0KO0RIACT
METHYLCHLOROISOTHIAZOLINONE/METHYLISOTHIAZOLINONE MIXTURE15O9QS218WIACT
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)59TL3WG5COIACT
AMMONIUM LAURETH-3 SULFATE896SJ235FNIACT

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
3da4be06-b8ea-460c-9e6f-2ba32a0ab61b143128c6-8c61-4dfd-ac2f-12892b9f7cb32019-07-15WarningsExact identifier
spl set id: 143128c6-8c61-4dfd-ac2f-12892b9f7cb3

Reported adverse events (FAERS/openFDA)#

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