Label: RELIEF- menthol patch
- NDC Code(s): 72587-002-01
- Packager: La Mend, Inc.
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated December 11, 2023
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- WHEN USING
- DO NOT USE
- STOP USE
- PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- STORAGE AND HANDLING
- INACTIVE INGREDIENT
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
RELIEF
menthol patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72587-002 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 5 g in 100 g Inactive Ingredients Ingredient Name Strength 2-ETHYLHEXYL ACRYLATE (UNII: HR49R9S6XG) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72587-002-01 1 in 1 BOX 04/15/2022 1 1 in 1 POUCH 1 1.35 g in 1 PATCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 04/15/2022 Labeler - La Mend, Inc. (117940830)