EPOCH AVA PUHI MONI ANTI-DANDRUFF- pyrithione zinc shampoo 
NSE Products, 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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Epoch® Ava Puhi Moni® Anti-Dandruff Shampoo

Drug Facts

Active Ingredients

Zinc Pyrithione 1%

Purpose

Anti-dandruff

Use

Controls the symptoms of dandruff.

Warning

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

  • Avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.

  • If condition worsens or does not improve after regular use of the product as directed, consult a doctor.

Directions

Inactive Ingredients

Water (Aqua), Ammonium Lauryl Sulfate, Ammonium Laureth Sulfate, Cocamide MIPA, Dimethicone, Zingiber Zerumbet Juice, Clematis Vitalba Leaf Extract, Mahonia Aquifolium Root Extract, Salvia Officinalis (Sage) Leaf Extract, Urtica Dioica (Nettle) Extract, Melia Azadirachta Leaf Extract, Panthenol, Butylene Glycol, Trisodium Ethylenediamine Disuccinate, Acrylates Copolymer, PEG/PPG-18/18 Dimethicone, Hexylene Glycol, Phenoxyethanol, Caprylyl Glycol, Ethylhexylglycerin, Citric Acid, Sodium Hydroxide, Fragrance (Parfum).

Questions?

1-888-742-7626

PRINCIPAL DISPLAY PANEL - 250 ml Bottle Label

epoch®

Ava puhi moni®

Anti-Dandruff
Shampoo

the "true ava puhi"

250 ml e (8.4 fl. oz.)

Principal Display Panel - 250 ml Bottle Label
EPOCH AVA PUHI MONI ANTI-DANDRUFF 
pyrithione zinc shampoo
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62839-6745
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5) PYRITHIONE ZINC65.7 g  in 1000 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
Ammonium Lauryl Sulfate (UNII: Q7AO2R1M0B)  
COCO MONOISOPROPANOLAMIDE (UNII: 21X4Y0VTB1)  
Dimethicone (UNII: 92RU3N3Y1O)  
Phenoxyethanol (UNII: HIE492ZZ3T)  
Caprylyl Glycol (UNII: 00YIU5438U)  
Sodium Hydroxide (UNII: 55X04QC32I)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
Trisodium Ethylenediamine Disuccinate (UNII: YA22H34H9Q)  
Ethylhexylglycerin (UNII: 147D247K3P)  
Hexylene Glycol (UNII: KEH0A3F75J)  
Panthenol (UNII: WV9CM0O67Z)  
AZADIRACHTA INDICA LEAF (UNII: HKY915780T)  
Butylene Glycol (UNII: 3XUS85K0RA)  
BERBERIS AQUIFOLIUM ROOT (UNII: 746TB9VNDP)  
CLEMATIS VITALBA LEAF (UNII: 526T95850X)  
PEG/PPG-18/18 Dimethicone (UNII: 9H0AO7T794)  
SAGE (UNII: 065C5D077J)  
URTICA DIOICA LEAF (UNII: X6M0DRN46Q)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:62839-6745-1250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/08/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart358H02/08/2017
Labeler - NSE Products, Inc. (803486393)

Revised: 1/2022
Document Id: faf5eb3a-7c3e-4a6c-b5c9-887883d341f5
Set id: a91a736a-f044-43e7-85f2-c5bcc5e57d50
Version: 2
Effective Time: 20220112
 
NSE Products, Inc.