PELO BAUM LASH LASH- allantoin liquid

Pelo Baum Lash Lash by

Drug Labeling and Warnings

Pelo Baum 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), Phenoxyethanol, Sodium Hyaluronate, Hydroxypropyl Methylcellulose, Glycerin, Arginine, Glycine Soja (Soybean) Oil, Disodium EDTA, Citric Acid, Hydrogenated Lecithin, Decapeptide-10, Oligopeptide-54, Decapeptide-18, Acetyl Decapeptide-3, Oligopeptide-42, Sodium Oleate, 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 25℃).

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN

Uses

Uses: Eyelash enhancer enriched with peptide complex, Helps to improve the appearance of natural lash length, fullness and thickness.

Directions

Directions: Apply a thin line of Pelo Baum Lash Lash to your cleansed upper lash line once a day at night, as though you were applying liquid eyeliner, leave it at least for 4 hours.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PELO BAUM LASH LASH 
allantoin liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 60716-090
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Phenoxyethanol (UNII: HIE492ZZ3T)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 60716-090-02	1 in 1 CARTON	06/01/2017
1	NDC: 60716-090-01	5 mL in 1 CONTAINER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part347	06/01/2017

Labeler - Caregen Co.,Ltd. (689850365)

Registrant - Caregen Co.,Ltd. (689850365)

Establishment
Name	Address	ID/FEI	Business Operations
Caregen Co.,Ltd.		689850365	manufacture(60716-090)