DOLL LASH- zinc pyrithione liquid

Doll Lash by

Drug Labeling and Warnings

Doll Lash by is a Otc medication manufactured, distributed, or labeled by Hanbit Korea. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient: Zinc pyrithione, Panthenol, Niacinamide, Biotin

INACTIVE INGREDIENT

Inactive ingredient: Acorus Calamus Root extract, Artemisia Absinthium extract, Methylparaben, thuja orientalis extract, Canavalia goadiata seed extract, Diazolidinyl urea

PURPOSE

For hair grower and loss prevention

KEEP OUT OF REACH OF CHILDREN

Keep this product out of the reach of children

INDICATIONS & USAGE

Directions for use: Apply six~seven times daily and every night onto clean skin.

                            For best results, use as often as possible.

                            It can be use in makeup

WARNINGS

1.When using Doll-Lash, avoid direct contact with the eyes, mucous membranes and open wounds.

2. If redness or imitation occurs, discontinue use and consult with your physician.

3. Keep this product out of the reach of children.

DOSAGE & ADMINISTRATION

Doll-Lash, Natural and vegetable property Eyelash , is our cosmetics product that enables short, weak, and thine eyelashes to be long, rich, healthy

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DOLL LASH 
zinc pyrithione liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51329-1001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5)	PYRITHIONE ZINC	2 mL  in 100 mL
PANTHENOL (UNII: WV9CM0O67Z) (PANTHENOL - UNII:WV9CM0O67Z)	PANTHENOL	0.5 mL  in 100 mL
NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4)	NIACINAMIDE	0.3 mL  in 100 mL
BIOTIN (UNII: 6SO6U10H04) (BIOTIN - UNII:6SO6U10H04)	BIOTIN	0.06 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ACORUS CALAMUS ROOT (UNII: XY1K7KIQ0F)
ARTEMISIA ABSINTHIUM FLOWERING TOP (UNII: F84709P2XV)
METHYLPARABEN (UNII: A2I8C7HI9T)
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51329-1001-1	8 mL in 1 BOTTLE, WITH APPLICATOR

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		11/06/2010

Labeler - Hanbit Korea (687524095)