LE K - CBD PURE CALM LAVENDER- benzalkonium chloride lotion

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]

ACTIVE INGREDIENT

Benzalkonium chloride 0.1%

PURPOSE

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

INDICATIONS & USAGE

To decrease bacteria on the skin.

DOSAGE & ADMINISTRATION

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

WARNINGS

For external use only.

KEEP OUT OF REACH OF CHILDREN

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

WHEN USING

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

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.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

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)
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)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
.BETA.-CITRONELLOL, (+/-)- (UNII: 565OK72VNF)
LINALOOL, (+/-)- (UNII: D81QY6I88E)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
COUMARIN (UNII: A4VZ22K1WT)
TRIDECETH-6 (UNII: 3T5PCR2H0C)
D&C VIOLET NO. 2 (UNII: 350KA7O6HK)
GERANIOL (UNII: L837108USY)
WATER (UNII: 059QF0KO0R)
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

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(82822-010)