FDA.reportPublic FDA data

LE K - ESSENTIAL-DM

Manufacturer
HCD ANTI AGING LABORATORIES LLC | CHEMCO CORPORATION
Effective date
2022-07-22
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:56:24

Label at a glance#

ProductLE K - ESSENTIAL-DM ALOE VERA
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

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

INACTIVE INGREDIENT SECTION

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 SECTION

To decrease bacteria on the skin.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

OTC - PURPOSE SECTION

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

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.1%

WARNINGS SECTION

For external use only.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

HCD - ESSENTIAL DM ALOE VERA ANTIBACTERIAL LOTIONHCD - ESSENTIAL DM ALOE VERA ANTIBACTERIAL LOTION

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
82822-001-012025-05-28C16284748780-12cef2736-820f-d83d-e063-dadaa90ab31f82822-001-01
82822-001-012025-01-30C16284748780-12cef2736-820f-d83d-e063-dadaa90ab31f82822-001-01

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 30 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82822-00182822-001-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 28 matching rows.

Name, UNII, Kind table
NameUNIIKind
CETYL ALCOHOL936JST6JCNIACT
STEARIC ACID4ELV7Z65APIACT
CAPRYLYL GLYCOL00YIU5438UIACT
PHENOXYETHANOLHIE492ZZ3TIACT
DIMETHICONE92RU3N3Y1OIACT
GLYCOL STEARATE0324G66D0EIACT
STEARYL ALCOHOL2KR89I4H1YIACT
.BETA.-CITRONELLOL, (+/-)-565OK72VNFIACT
LINALOOL, (+/-)-D81QY6I88EIACT
HEXYLENE GLYCOLKEH0A3F75JIACT
ALPHA-TOCOPHEROL ACETATE9E8X80D2L0IACT
GREEN TEA LEAFW2ZU1RY8B0IACT
ARNICA MONTANA FLOWEROZ0E5Y15PZIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
.ALPHA.-HEXYLCINNAMALDEHYDE7X6O37OK2IIACT
.ALPHA.-AMYLCINNAMALDEHYDEWC51CA3418IACT
HYDROXYCITRONELLAL8SQ0VA4YURIACT
COUMARINA4VZ22K1WTIACT
TRIDECETH-63T5PCR2H0CIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
GLYCERETH-26NNE56F2N14IACT
SODIUM HYDROXIDE55X04QC32IIACT
ROSEMARYIJ67X351P9IACT
GERANIOLL837108USYIACT
VITIS VINIFERA SEEDC34U15ICXAIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
WATER059QF0KO0RIACT
MINERAL OILT5L8T28FGPIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
362ab448-8259-19c7-e063-6394a90a0149e34f6b5e-a25c-ae2d-e053-2a95a90a66112025-05-27WarningsExact identifier
spl set id: e34f6b5e-a25c-ae2d-e053-2a95a90a6611

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.