Label: DESERT HARVEST RELEVEUM- lidocaine cream
- NDC Code(s): 69145-201-04, 69145-201-08
- Packager: Desert Harvest Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 5, 2023
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- Desert Harvest RELEVEUM
- Active Ingredients:
- Uses:
- Warnings:
- Directions:
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Inactive ingredients
Deionized Water, Certified Organic Aloe Barbadensis Leaf Juice, Glyceryl Stearate (Natural Skin Lubricant), Stearic Acid (Plant-based Fatty Acid), Cartharnus Tinctorius (Safflower) Seed Oil, Rosa Canina (Rosehips) Fruit Oil, Sodium Ascorbyl Phosphate (Vitamin C), Salvia Sin-ensis (Chia) Seed Oil, Vegetable Glycerin, Cetyl Alcohol (from Coconut Oil), Carbomer (Natural Thickener), Calendula Officitialis (Pot Marigold) Flower i Extract, Chamomilla Recutita (Chamomile) Flower Extract, Matrlcarla Cha-mornilla (Roman Chamomile) Flower Extract, Tilia Oficinalis (Linden) Ex-tract, Hypericum Perforatum (St. John's Wort) Extract, Centaurea Cyanus (Cornflower) Extract, Vitis Vinifera (Grape) Seed Extract, Tabebuia Impetiginosa (Pau d'Arco) Extract, Camellia Oleifera (Japanese Green Tea) Leaf Extract, Tocopheryl Acetate (Vitamin E), Leuconostoc/Radish Root Ferment Filtrate (Natural Antimicrobial), Lonicera Japonica (Honeysuckle) Flower Extract, Lonicera Caprifolium (Honeysuckle) Extract, Populus Tremuloides (Aspen) Bark Extract, Gluconolactone (Natural Skin Conditioner)
- Desert Harvest RELEVEUM
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INGREDIENTS AND APPEARANCE
DESERT HARVEST RELEVEUM
lidocaine creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69145-201 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE 40 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALOE VERA LEAF (UNII: ZY81Z83H0X) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) STEARIC ACID (UNII: 4ELV7Z65AP) SAFFLOWER OIL (UNII: 65UEH262IS) ROSA CANINA FRUIT OIL (UNII: CR7307M3QZ) SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR) CHIA SEED OIL (UNII: MC2LH51BO7) GLYCERIN (UNII: PDC6A3C0OX) CETYL ALCOHOL (UNII: 936JST6JCN) CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD) CHAMOMILE (UNII: FGL3685T2X) CHAMAEMELUM NOBILE FLOWER (UNII: O2T154T6OG) TILIA CORDATA FLOWER (UNII: CFN6G1F6YK) ST. JOHN'S WORT (UNII: UFH8805FKA) CENTAUREA CYANUS FLOWER (UNII: QZ239038YC) VITIS VINIFERA SEED (UNII: C34U15ICXA) TABEBUIA IMPETIGINOSA WHOLE (UNII: D65QWF3541) CAMELLIA OLEIFERA LEAF (UNII: 5077EL0C60) .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1) LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE (UNII: D2QHA03458) LONICERA JAPONICA FLOWER (UNII: 4465L2WS4Y) LONICERA CAPRIFOLIUM FLOWER (UNII: 5N1WD9784U) POPULUS TREMULOIDES BARK (UNII: 5543O0CEID) GLUCONOLACTONE (UNII: WQ29KQ9POT) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69145-201-04 118 mL in 1 BOTTLE; Type 0: Not a Combination Product 02/06/2017 2 NDC:69145-201-08 236 mL in 1 BOTTLE; Type 0: Not a Combination Product 02/06/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 07/30/2014 Labeler - Desert Harvest Inc. (034527161) Establishment Name Address ID/FEI Business Operations Pure Source, LLC 080354456 manufacture(69145-201)
