RENOKIN LASH LASH- allantoin liquid

RENOKIN LASH LASH by

Drug Labeling and Warnings

RENOKIN LASH LASH by is a Otc medication manufactured, distributed, or labeled by Caregen Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient: Allantoin 0.5%

INACTIVE INGREDIENT

Inactive ingredients:
Water (Aqua), Alcohol, Glycerin, Isopropyl Alcohol, Phenoxyethanol, Ginkgo Biloba Leaf Extract, Glycine Soja (Soybean) Oil, Hydrogenated Lecithin, Thuja Orientalis Extract, Disodium EDTA, Oligopeptide-54, Decapeptide-18, Serenoa Serrulata Fruit Extract, Polygala Tenuifolia Root Extract, Portulaca Oleracea Extract, Fragrance (Parfum), Decapeptide-10, Sodium Oleate, Retinyl Palmitate, Biotin

PURPOSE

Purpose: Skin Protectant

WARNINGS

Warning:
For external use only, do not swallow.
In case of accidental ingestion, seek medical assistance.
Avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.
Stop use and consult a doctor if rash or irritation occurs.
Do not apply directly to a wound or open cut.
Keep out of reach of children.
Store at room temperature (below 25C).

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN

INDICATIONS AND USAGE

Directions:
Apply a thin line of RENOKIN lashlash to your upper lash line once a day at night on a cleansed face, as though you were applying liquid eyeliner.
Leave it at least for 4 hours.

DOSAGE AND ADMINISTRATION

Directions:
Apply a thin line of RENOKIN lashlash to your upper lash line once a day at night on a cleansed face, as though you were applying liquid eyeliner.
Leave it at least for 4 hours.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

RENOKIN LASH LASH 
allantoin liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 60716-040
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Allantoin (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z)	Allantoin	0.025 mg  in 5 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Glycerin (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 60716-040-01	5 mL in 1 CARTON

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part347	03/07/2014

Labeler - Caregen Co., Ltd. (689850365)

Registrant - Caregen Co., Ltd. (689850365)

Establishment
Name	Address	ID/FEI	Business Operations
Caregen Co., Ltd.		689850365	manufacture(60716-040)