Label: COPPERLIFE PAIN RELIEF LIQUID- menthol 16% spray
- NDC Code(s): 72562-121-25
- Packager: Tommie Copper, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 15, 2024
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
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WARNINGS
For external use only. Flammable--Keep away from fire or flame. When using this product avoid contact with eyes. In case of contact with eyes, flush thoroughly with water, do not apply to wounds or damaged skin, and do not bandage tightly, do not use with a heating pad. Contents under pressure. Do not puncture or incinerate. Do not store at temperature above 120F. . Stop use and ask a doctor if condition worsens, if symptoms persist for more than 7 days or clear up and occur again within a few days.
- PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
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INACTIVE INGREDIENT
Alcohol Denat., Aloe Barbadensis (Aloe Vera) Leaf Extract, Anthemis Nobilis (Roman Chamomile) Flower Oil, Arnica Montana (Arnica) Flower Extract, Boswellia Serrata (Frankincense) Extract, Cannabis Sativa (Hemp) Extract, Capsicum Annuum (Paprika) Extract, Citrus Limon (Lemon) Peel Oil, Curcuma Longa (Tumeric) Root Extract, Glycerin, Lavandula Angustifolia (Lavender) Oil, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Propylene Glycol, Salix Alba (Willow) Bark Extract, Trifolium Pratense (Clover) Flower Extract, Water, Zingiber Officinale (Ginger) Root Extract
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
COPPERLIFE PAIN RELIEF LIQUID
menthol 16% sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72562-121 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 16 g in 100 g Inactive Ingredients Ingredient Name Strength LAVENDER OIL (UNII: ZBP1YXW0H8) TEA TREE OIL (UNII: VIF565UC2G) SALIX ALBA BARK (UNII: 205MXS71H7) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) CALENDULA ARVENSIS LEAF (UNII: 3U3U118F2L) WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) ALOE VERA LEAF (UNII: ZY81Z83H0X) ALCOHOL (UNII: 3K9958V90M) INDIAN FRANKINCENSE (UNII: 4PW41QCO2M) CANNABIS SATIVA FLOWERING TOP (UNII: 8X454SZ22D) PAPRIKA (UNII: X72Z47861V) ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ) LEMON OIL, COLD PRESSED (UNII: I9GRO824LL) CHAMAEMELUM NOBILE FLOWER OIL (UNII: UB27587839) TRIFOLIUM PRATENSE FLOWER (UNII: 4JS0838828) GINGER (UNII: C5529G5JPQ) TURMERIC (UNII: 856YO1Z64F) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72562-121-25 70 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 08/10/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 08/10/2021 Labeler - Tommie Copper, Inc. (081176569) Registrant - Derma Care Research Labs, LLC (116817470) Establishment Name Address ID/FEI Business Operations Derma Care Research Labs, LLC 116817470 manufacture(72562-121)
