Label: THERMACARE HEAT THERAPY MAX STRENGTH LIDOCAINE PAIN RELIEF ROLLON liquid
- NDC Code(s): 69693-002-25
- Packager: Clarion Brands LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 26, 2025
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
-
WARNINGS
For external use only
Flammable keep away from heat and open flame
Do not use
- in large quantities
- on wounds, damaged, broken, or irritated skin
- for more than one week without consulting a doctor
When using this product
- use only as directed. Read and follow all directions and warnings on this label
- avoid contact with the eyes and mucous membranes
- do not bandage tightly or apply local heat such as a heating pad or a medicated patch
- do not use with other topical analgesics
Stop use and ask a doctor if
- rash or irritation develops
- symptoms worsen or persist for more than 7 days or clear up and occur again within a few days
If pregnant or breast-feeding, ask a health professional before use.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
- WHEN USING
- INACTIVE INGREDIENT
- QUESTIONS
- DOSAGE & ADMINISTRATION
- KEEP OUT OF REACH OF CHILDREN
-
PRINCIPAL DISPLAY PANEL
Thermacare Heat Therapy
Heat + Max Strength Lidocaine Pain Relief
Roll On NET WT 2.5 OZ (70 g)
No Mess Applicator
Vanishing Scent
Start with Small Amount; Skin Sensitivity Varies
Distributed by: Bridges Consumer Healthcare
811 Broad Street, Suite 600
Chattanooga, TN 37402
2026 Bridges CHC
Thermacare.com
-
INGREDIENTS AND APPEARANCE
THERMACARE HEAT THERAPY MAX STRENGTH LIDOCAINE PAIN RELIEF ROLLON
thermacare heat therapy max strength lidocaine pain relief rollon liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69693-002 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS 4 g in 100 mL BENZYL ALCOHOL (UNII: LKG8494WBH) (BENZYL ALCOHOL - UNII:LKG8494WBH) BENZYL ALCOHOL 10 g in 100 mL Inactive Ingredients Ingredient Name Strength POLYACRYLATE CROSSPOLYMER-6 (UNII: Q7UI015FF9) VANILLYL BUTYL ETHER (UNII: S2ULN37C9R) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) CAPRYLYL GLYCOL (UNII: 00YIU5438U) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) EDETATE DISODIUM (UNII: 7FLD91C86K) HYDROXYETHYLCELLULOSE (UNII: T4V6TWG28D) WATER (UNII: 059QF0KO0R) BISABOLOL (UNII: 24WE03BX2T) ALOE BARBADENSIS LEAF JUICE (UNII: RUE8E6T4NB) AMINOMETHYLPROPANOL (UNII: LU49E6626Q) GINGER (UNII: C5529G5JPQ) ALCOHOL (UNII: 3K9958V90M) MALTODEXTRIN (UNII: 7CVR7L4A2D) Product Characteristics Color Score Shape ROUND Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69693-002-25 1 mL in 1 BOTTLE; Type 0: Not a Combination Product 11/15/2025 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 11/15/2025 Labeler - Clarion Brands LLC (079742703)