- Drug Facts
- Active ingredient:
- Purpose
- Uses
-
Warnings:
For external use only
When using this product
Do not bandage tightly • avoid contact with eyes • do not apply to wounds or damaged skin • do not use with heating pads or other heating devices.
Stop use and ask a doctor if
• Condition worsens or if symptoms persist for more than 7 days or clear up and occur again within a few days
- Keep out of reach of children.
- Directions
- Inactive ingredients:
- QUESTIONS
- SPL UNCLASSIFIED SECTION
- Packaging
-
INGREDIENTS AND APPEARANCE
EEZ-AWAY PAIN RELIEF
menthol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69678-111 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL, UNSPECIFIED FORM 2.5 g in 100 mL Inactive Ingredients Ingredient Name Strength ISOPROPYL ALCOHOL (UNII: ND2M416302) WATER (UNII: 059QF0KO0R) PEG-75 LANOLIN (UNII: 09179OX7TB) POLYOXYL-10 OLEYL ETHER (UNII: JD797EF70J) PPG-20 METHYL GLUCOSE ETHER (UNII: 3WV1T97D3K) IODINE (UNII: 9679TC07X4) SODIUM IODIDE (UNII: F5WR8N145C) ALCOHOL (UNII: 3K9958V90M) SODIUM THIOSULFATE (UNII: HX1032V43M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69678-111-02 84 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/24/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 10/24/2018 Labeler - EEZAWAY RELIEF INC (079751465)