Label: COPPERLIFE PAIN RELIEF- trolamine salicylate 10% cream
- NDC Code(s): 72562-123-25
- 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. Allergy Alert: If prone to allergic reaction from aspirin or salicylates, consult a doctor before use. . When using this product use only as directed, do not bandage tightly or use with a heating pad, avoid 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
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, Cetyl Alcohol, Citrus Limon (Lemon) Peel Oil, Curcuma Longa (Tumeric) Root Extract, Glycerin, Lavandula Angustifolia (Lavender) Oil, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Methylparaben, Mineral Oil, Potassium Phosphate, Propylparaben, Salix Alba (Willow) Bark Extract, Stearic Acid, Triethanolamine, Trifolium Pratense (Clover) Flower Extract, Water, Zingiber Officinale (Ginger) Root Extract.
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
COPPERLIFE PAIN RELIEF
trolamine salicylate 10% creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72562-123 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TROLAMINE SALICYLATE (UNII: H8O4040BHD) (SALICYLIC ACID - UNII:O414PZ4LPZ) TROLAMINE SALICYLATE 10 g in 100 g Inactive Ingredients Ingredient Name Strength TROLAMINE (UNII: 9O3K93S3TK) MINERAL OIL (UNII: T5L8T28FGP) METHYLPARABEN (UNII: A2I8C7HI9T) TRIFOLIUM PRATENSE FLOWER (UNII: 4JS0838828) GINGER (UNII: C5529G5JPQ) SALIX ALBA BARK (UNII: 205MXS71H7) PROPYLPARABEN (UNII: Z8IX2SC1OH) CHAMAEMELUM NOBILE FLOWER OIL (UNII: UB27587839) WATER (UNII: 059QF0KO0R) POTASSIUM PHOSPHATE, MONOBASIC (UNII: 4J9FJ0HL51) STEARIC ACID (UNII: 4ELV7Z65AP) GLYCERIN (UNII: PDC6A3C0OX) ALOE VERA LEAF (UNII: ZY81Z83H0X) ISOPROPYL ALCOHOL (UNII: ND2M416302) INDIAN FRANKINCENSE (UNII: 4PW41QCO2M) CANNABIS SATIVA SEED (UNII: QE567Z26NG) CETYL ALCOHOL (UNII: 936JST6JCN) ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ) PAPRIKA (UNII: X72Z47861V) LEMON OIL (UNII: I9GRO824LL) TURMERIC (UNII: 856YO1Z64F) TEA TREE OIL (UNII: VIF565UC2G) LAVENDER OIL (UNII: ZBP1YXW0H8) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72562-123-25 70 g in 1 TUBE; Type 0: Not a Combination Product 08/11/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 08/11/2021 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(72562-123)