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Progenesis

Manufacturer
Palcare Enterprises Inc
Effective date
2023-01-10
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:41:16

Label at a glance#

ProductProgenesis
Active ingredientPYRITHIONE ZINC
Label structure10 sections

Dosage and administration

• Wet hair with warm water, • Apply 4-5 drops of the product, • Massage gently into the lather of your scalp and hair and allow to act for a few minutes • Subsequently rinse accurately.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Zinc Pyrithione..... 0.5%

Purpose

OTC - PURPOSE SECTION

Anti-Dandruff

Use

INDICATIONS & USAGE SECTION

Removes thin and dry dandruff flakes, nourishes and moisturizes the scalp.

Warnings

WARNINGS SECTION

  • For external use only
  • In case of eye contact, wash immediately

Do not use

OTC - DO NOT USE SECTION

Do not use it on an open wounds or cuts

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

• Wet hair with warm water,

• Apply 4-5 drops of the product,

• Massage gently into the lather of your scalp and hair and allow to act for a few minutes

• Subsequently rinse accurately.

OTC - QUESTIONS SECTION

Questions (or comments)? Call 1-250-590-4850

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, sodium laureth sulfate, cocamidopropyl betaine, PEG-150 pentaerythrityl tetrastearate, PPG-2 hydroxyethyl cocamide, sodium benzoate polysorbate 20, parfum, citric acid, cocamide DEA, piroctone olamine, sodium naphthalenesulfonate, capsicum frutescens fruit extract, propylene glycol, achillea millefolium extract, 1,2-hexanediol, sodium cocoamphoacetate, polyquaternium-7, dipropylene glycol, propanediol, panthenol, potassium sorbate, glycerin, sodium chloride

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

250 mL NDC: 82349-139-65250 mL NDC: 82349-139-65

250 mL NDC: 82349-139-65

Products#

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

DailyMed product names page 1 of 1 · 26 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82349-13982349-139-65

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 24 matching rows.

Name, UNII, Kind table
NameUNIIKind
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
PENTAERYTHRITYL TETRASTEARATEW9Q3DZS0EGIACT
SODIUM NAPHTHALENESULFONATED3F8YRX7TPIACT
TABASCO PEPPERJ1M3NA843LIACT
PROPANEDIOL5965N8W85TIACT
PANTHENOLWV9CM0O67ZIACT
GLYCERINPDC6A3C0OXIACT
DIPROPYLENE GLYCOLE107L85C40IACT
POTASSIUM SORBATE1VPU26JZZ4IACT
SODIUM CHLORIDE451W47IQ8XIACT
COCO DIETHANOLAMIDE92005F972DIACT
1,2-HEXANEDIOLTR046Y3K1GIACT
POLYSORBATE 207T1F30V5YHIACT
PIROCTONE OLAMINEA4V5C6R9FBIACT
SODIUM BENZOATEOJ245FE5EUIACT
POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600 KD)0L414VCS5YIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
SODIUM COCOAMPHOACETATEW7Q5E87674IACT
PPG-2 HYDROXYETHYL COCAMIDE34N07GUJ3XIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
PEG-150 LANOLIN8WTH94XZF2IACT
SODIUM LAURETH SULFATEBPV390UAP0IACT
PYRITHIONE ZINCR953O2RHZ5ACTIB
ACHILLEA MILLEFOLIUM2FXJ6SW4PKIACT

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
ffa24e1a-9d56-f43e-e053-6394a90a8018d2039edf-8962-0bca-e053-2995a90a17d62023-07-03WarningsExact identifier
spl set id: d2039edf-8962-0bca-e053-2995a90a17d6

Reported adverse events (FAERS/openFDA)#

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