Label: AROMALIEF CALMING PAIN RELIEF CREAM LAVENDER- menthol lotion
- NDC Code(s): 72393-302-02, 72393-302-04
- Packager: Marketites LLC
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated January 10, 2023
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- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- Warnings
- Directions
- Ohter Information
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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
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INGREDIENTS AND APPEARANCE
AROMALIEF CALMING PAIN RELIEF CREAM LAVENDER
menthol lotionProduct 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 not final part348 08/01/2020 Labeler - Marketites LLC (036140212)