Label: RELIEF- menthol patch
- NDC Code(s): 72587-003-01
- Packager: La Mend, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated August 1, 2024
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- Official Label (Printer Friendly)
- Active ingredients
- Purpose
- Uses
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Warnings
For external use only
When using this product
- use only as directed
- avoid contact with the eyes and other mucous membranes
- do not apply to wounds or damaged skin
- do not bandage tightly
- use only as directed
- Directions
- Other information
- Inactive ingredients
- Questions or Comments
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
RELIEF
menthol patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72587-003 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 LAVENDER OIL (UNII: ZBP1YXW0H8) ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ) EUCALYPTUS OIL (UNII: 2R04ONI662) ALOE VERA LEAF (UNII: ZY81Z83H0X) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72587-003-01 4 in 1 POUCH 08/01/2024 1 1 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 08/01/2024 Labeler - La Mend, Inc. (117940830) Establishment Name Address ID/FEI Business Operations Akron Coating & Adhesives 186569323 manufacture(72587-003)