LE K - CBD PURE CALM by HCD ANTI AGING LABORATORIES LLC / CHEMCO CORPORATION 82822-010-01

LE K - CBD PURE CALM by

Drug Labeling and Warnings

LE K - CBD PURE CALM 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]

LE K - CBD PURE CALM LAVENDER- benzalkonium chloride lotion 
HCD ANTI AGING LABORATORIES LLC

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82822-010-01

Benzalkonium chloride 0.1%

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

To decrease bacteria on the skin.

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

For external use only.

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

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.

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.

LE K - CBD PURE CALM  LAVENDER
benzalkonium chloride lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82822-010
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
LIMONENE, (+)- (UNII: GFD7C86Q1W)
BENZYL SALICYLATE (UNII: WAO5MNK9TU)
LAVENDER OIL (UNII: ZBP1YXW0H8)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
BENZYL BENZOATE (UNII: N863NB338G)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
OAT (UNII: Z6J799EAJK)
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CANNABIDIOL (UNII: 19GBJ60SN5)
CHAMOMILE (UNII: FGL3685T2X)
CETYL ALCOHOL (UNII: 936JST6JCN)
STEARIC ACID (UNII: 4ELV7Z65AP)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
.BETA.-CITRONELLOL, (+/-)- (UNII: 565OK72VNF)
LINALOOL, (+/-)- (UNII: D81QY6I88E)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
WATER (UNII: 059QF0KO0R)
COUMARIN (UNII: A4VZ22K1WT)
TRIDECETH-6 (UNII: 3T5PCR2H0C)
D&C VIOLET NO. 2 (UNII: 350KA7O6HK)
GERANIOL (UNII: L837108USY)
MINERAL OIL (UNII: T5L8T28FGP)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)

Product Characteristics
Color	purple	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82822-010-01	25 g in 1 POUCH; Type 0: Not a Combination Product	07/22/2022	04/06/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	07/22/2022	04/06/2025

Labeler - HCD ANTI AGING LABORATORIES LLC (118675977)

Revised: 5/2025

Document Id: 362ad462-231e-4218-e063-6294a90afacd

34390-5

Set id: e4685baf-e0fa-eb37-e053-2a95a90a6dea

Version: 2

Effective Time: 20250527