FDA.reportPublic FDA data

LE K - CBD PURE CALM

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 21:56:21

Label at a glance#

ProductLE K - CBD PURE CALM LAVENDER
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.1%

OTC - PURPOSE SECTION

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

INDICATIONS & USAGE SECTION

To decrease bacteria on the skin.

DOSAGE & ADMINISTRATION SECTION

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

WARNINGS SECTION

For external use only.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

OTC - WHEN USING SECTION

Avoid contact with the eyes.
Do not apply to wounds or damaged skin.

Do not apply to the irritated skin or if excessive irritation develops.

INACTIVE INGREDIENT SECTION

Aqua, Paraffinum Liquidum, Stearic Acid, Cetyl Alcohol, Caprylyl Glycol, Hexylene Glycol, Phenoxyethanol, Sodium Hydroxide, Parfum, Acrylamide/Sodium Acrylate Copolymer, Trideceth-6, Stearyl Alcohol, Propylene Glycol, Titanium Dioxide, Cannabidiol, Avena Sativa Kernel Extract, Glycerin, Chamomilla Recutita (Matricaria) Flower Extract, Lavandula Angustifolia (Lavender) Oil, D&C Violet #2 (CI 60730), Linalool, Benzyl Benzoate, Limonene, Benzyl Salicylate, Coumarin, Geraniol, Citronellol.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

HCD - PURE CALM LAVENDER LOTIONHCD - PURE CALM LAVENDER LOTION

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
82822-010-012025-05-28C16284748780-12cef2736-87e3-d83d-e063-dadaa90ab31f82822-010-01
82822-010-012025-01-30C16284748780-12cef2736-87e3-d83d-e063-dadaa90ab31f82822-010-01

Products#

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

DailyMed product names page 1 of 1 · 28 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82822-01082822-010-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 26 matching rows.

Name, UNII, Kind table
NameUNIIKind
LIMONENE, (+)-GFD7C86Q1WIACT
BENZYL SALICYLATEWAO5MNK9TUIACT
LAVENDER OILZBP1YXW0H8IACT
BENZYL BENZOATEN863NB338GIACT
TITANIUM DIOXIDE15FIX9V2JPIACT
OATZ6J799EAJKIACT
GLYCERINPDC6A3C0OXIACT
SODIUM HYDROXIDE55X04QC32IIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
CANNABIDIOL19GBJ60SN5IACT
CHAMOMILEFGL3685T2XIACT
CETYL ALCOHOL936JST6JCNIACT
STEARIC ACID4ELV7Z65APIACT
PHENOXYETHANOLHIE492ZZ3TIACT
STEARYL ALCOHOL2KR89I4H1YIACT
.BETA.-CITRONELLOL, (+/-)-565OK72VNFIACT
LINALOOL, (+/-)-D81QY6I88EIACT
HEXYLENE GLYCOLKEH0A3F75JIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
COUMARINA4VZ22K1WTIACT
TRIDECETH-63T5PCR2H0CIACT
D&C VIOLET NO. 2350KA7O6HKIACT
GERANIOLL837108USYIACT
WATER059QF0KO0RIACT
MINERAL OILT5L8T28FGPIACT
CAPRYLYL GLYCOL00YIU5438UIACT

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
362ad462-231e-4218-e063-6294a90afacde4685baf-e0fa-eb37-e053-2a95a90a6dea2025-05-27WarningsExact identifier
spl set id: e4685baf-e0fa-eb37-e053-2a95a90a6dea

Reported adverse events (FAERS/openFDA)#

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