LE K - ESSENTIAL-DM ALOE VERA- benzalkonium chloride lotion

LE K - ESSENTIAL-DM by

Drug Labeling and Warnings

LE K - ESSENTIAL-DM by is a Otc medication manufactured, distributed, or labeled by HCD ANTI AGING LABORATORIES LLC, CHEMCO CORPORATION. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DOSAGE & ADMINISTRATION

Apply product on hands as needed. Rub hands together until absorbed.

INACTIVE INGREDIENT

Aqua, Paraffinum Liquidum, Stearic Acid, Cetyl Alcohol, Caprylyl Glycol, Hexylene Glycol, Phenoxyethanol, Glycereth-26, Dimethicone, Glycol Stearate, Acrylamide/Sodium Acrylate Copolymer, Trideceth-6, Sodium Hydroxide, Stearyl Alcohol, Parfum, Tocopheryl Acetate, Camelia Sinensis Extract, Rosmarinus Officinalis (Rosemary) Extract, Arnica Montana Flower Extract, Vitis Vinifera (Grape) Seed Extract, Propylene Glycol, FD&C Blue #1 (CI 42090), Geraniol, Hexyl Cinnamal, Amyl Cinnamal, Citronellol, Hydroxycitronnellal, Linalool, Coumarin.

INDICATIONS & USAGE

To decrease bacteria on the skin.

KEEP OUT OF REACH OF CHILDREN

If swallowed, get medical help or contact a Poison Control Center right away.

PURPOSE

Benzalkonium chloride 0.1%………………….….…………………………………………………………Antibacterial

ACTIVE INGREDIENT

Benzalkonium chloride 0.1%

WARNINGS

For external use only.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

LE K - ESSENTIAL-DM  ALOE VERA
benzalkonium chloride lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82822-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.1 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
CETYL ALCOHOL (UNII: 936JST6JCN)
STEARIC ACID (UNII: 4ELV7Z65AP)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
DIMETHICONE (UNII: 92RU3N3Y1O)
GLYCOL STEARATE (UNII: 0324G66D0E)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
.BETA.-CITRONELLOL, (+/-)- (UNII: 565OK72VNF)
LINALOOL, (+/-)- (UNII: D81QY6I88E)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
.ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
.ALPHA.-AMYLCINNAMALDEHYDE (UNII: WC51CA3418)
HYDROXYCITRONELLAL (UNII: 8SQ0VA4YUR)
COUMARIN (UNII: A4VZ22K1WT)
TRIDECETH-6 (UNII: 3T5PCR2H0C)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
GLYCERETH-26 (UNII: NNE56F2N14)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
ROSEMARY (UNII: IJ67X351P9)
GERANIOL (UNII: L837108USY)
VITIS VINIFERA SEED (UNII: C34U15ICXA)
WATER (UNII: 059QF0KO0R)
MINERAL OIL (UNII: T5L8T28FGP)

Product Characteristics
Color	blue	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82822-001-01	25 g in 1 POUCH; Type 0: Not a Combination Product	07/22/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	07/22/2022

Labeler - HCD ANTI AGING LABORATORIES LLC (118675977)

Establishment
Name	Address	ID/FEI	Business Operations
CHEMCO CORPORATION		032495954	manufacture(82822-001)