Label: TOMMIE COPPER PAIN RELIEF- trolamine salicylate 10% cream
- NDC Code(s): 72562-223-25
- 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, Arnica Montana (Arnica) Flower Extract, Calendula Officinalis (Marigold) Flower Extract, Camellia Sinensis (Green Tea) Leaf Extract, Cetyl Alcohol, Chamomilla Recutita (Matricaria) Flower Extract, Cucumis Sativus (Cucumber) Fruit Extract, Echinacea Angustifolia (Coneflower) Extract, Glycerin, Ilex Paraguariensis (Yerba Mate) Leaf Extract, Juniperus Communis (Juniper) Fruit Extract, Mentha Piperita (Peppermint) Oil, Methylparaben, Mineral Oil, Potassium Phosphate, Propylparaben, Stearic Acid, Triethanolamine, Water.
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
TOMMIE COPPER PAIN RELIEF
trolamine salicylate 10% creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72562-223 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) CHAMOMILE (UNII: FGL3685T2X) GREEN TEA LEAF (UNII: W2ZU1RY8B0) CUCUMBER (UNII: YY7C30VXJT) PROPYLPARABEN (UNII: Z8IX2SC1OH) CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD) WATER (UNII: 059QF0KO0R) POTASSIUM PHOSPHATE, MONOBASIC (UNII: 4J9FJ0HL51) STEARIC ACID (UNII: 4ELV7Z65AP) GLYCERIN (UNII: PDC6A3C0OX) ALOE VERA LEAF (UNII: ZY81Z83H0X) ECHINACEA ANGUSTIFOLIA LEAF (UNII: FS7G8S6PJ8) ILEX PARAGUARIENSIS LEAF (UNII: 1Q953B4O4F) CETYL ALCOHOL (UNII: 936JST6JCN) ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ) JUNIPER BERRY (UNII: O84B5194RL) PEPPERMINT OIL (UNII: AV092KU4JH) METHYLPARABEN (UNII: A2I8C7HI9T) LAVENDER OIL (UNII: ZBP1YXW0H8) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72562-223-25 70 g in 1 TUBE; Type 0: Not a Combination Product 08/19/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 08/19/2021 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(72562-223)