EPOCH AVA PUHI MONI ANTI-DANDRUFF- pyrithione zinc shampoo

Epoch Ava Puhi Moni Anti-Dandruff by

Drug Labeling and Warnings

Epoch Ava Puhi Moni Anti-Dandruff by is a Otc medication manufactured, distributed, or labeled by NSE Products, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredients

Zinc Pyrithione 1%

Purpose

Anti-dandruff

Use

Controls the symptoms of dandruff.

Warning

• For external use only

• 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

• Wet hair, lather thoroughly
• Leave in 1–2 minutes and rinse well
• For best results, use daily or at least twice a week (or as directed by a doctor).

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.)

INGREDIENTS AND APPEARANCE

EPOCH AVA PUHI MONI ANTI-DANDRUFF 
pyrithione zinc shampoo

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62839-6745
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5)	PYRITHIONE ZINC	65.7 g  in 1000 mL

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62839-6745-1	250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/08/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH FINAL	part358H	02/08/2017

Labeler - NSE Products, Inc. (803486393)