AROMALIEF CALMING PAIN RELIEF CREAM LAVENDER- menthol lotion

Aromalief Calming Pain Relief Cream Lavender by

Drug Labeling and Warnings

Aromalief Calming Pain Relief Cream Lavender by is a Otc medication manufactured, distributed, or labeled by Marketites LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredients

Menthol 1.0% w/w

PURPOSE

Topical Analgesic

INDICATIONS & USAGE

Use For temporary relief of pain

Warnings

Warnings

For external use only. Avoid contact with eyes.

Stop use and ask a doctor if condition worsens, symptoms persist for more than 7 days, or new symptoms occur.

Keep out of reach of children, if swallowed, get medical help or contact a Poison Control Center right away. If pregnant or breastfeeding, ask a health professional.

Directions

Adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times daily. Children under 2 years of age: consult a doctor.

Ohter Information

Store in a cool dry place between 68º and 77ºF and relative humidity not exceeding 65%.

Do not use if seal is broken, torn or missing.

Inactive Ingredients

Aloe Barbadensis Leaf Extract, Water, Stearyl Alcohol, Prunus Amygdalus Dulcis (Sweet Almond) Oil, Isopropyl Myristate, Glyceryl Stearate, Menthyl Lactate, Glycerin, PEG 100 Stearate, Cannabis Sativa Seed Oil, Ulva lactuca Linnaeus, Fucaceae Fucus Vesiculosus, Sodium Hyaluronate, Helianthus Annuus (Sunflower) Seed Oil, Fragrance, Lavandula Angustifolia (Lavender) Flower Oil, Maltodextrin, Glucosamine Sulfate, Dimethyl Sulfone (MSM), L-Arginine, Glycol Stearate, Phenoxyethanol, Caprylyl Glycol

Questions

Distributed by Marketites LLC

Coral Gables, FL 33134

Made in the USA

Questions? info@aromalief.com

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

AROMALIEF CALMING PAIN RELIEF CREAM LAVENDER 
menthol lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72393-302
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	1 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
GLUCOSAMINE SULFATE (UNII: 1FW7WLR731)
MENTHYL LACTATE, (-)- (UNII: 2BF9E65L7I)
GLYCERIN (UNII: PDC6A3C0OX)
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
ARGININE (UNII: 94ZLA3W45F)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
GLYCOL STEARATE (UNII: 0324G66D0E)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
WATER (UNII: 059QF0KO0R)
LAVANDULA ANGUSTIFOLIA FLOWER (UNII: 19AH1RAF4M)
ULVA LACTUCA (UNII: PHR3P25W6Y)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ALMOND OIL (UNII: 66YXD4DKO9)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
PEG-100 STEARATE (UNII: YD01N1999R)
CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)
FUCUS VESICULOSUS (UNII: 535G2ABX9M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72393-302-04	0.14 g in 1 TUBE; Type 0: Not a Combination Product	08/01/2020
2	NDC: 72393-302-02	0.07 g in 1 TUBE; Type 0: Not a Combination Product	08/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	08/01/2020

Labeler - Marketites LLC (036140212)