Label: MEDICATED PAIN RELIEF- menthol patch
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Contains inactivated NDC Code(s)
NDC Code(s): 67510-1301-5 - Packager: Kareway Product, Inc.
- Category: HUMAN OTC DRUG LABEL
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated March 7, 2019
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Uses
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Warnings
For external use only
When using this product
- use only as directed
- do not bandage tightly or use a heating pad
- avoid contact with eyes and mucous membrane
- do not apply to wounds or damaged skin
- Directions
- Other Information
- Inactive ingredients
- package label
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INGREDIENTS AND APPEARANCE
MEDICATED PAIN RELIEF
menthol patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:67510-1301 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 400 mg Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L) DIHYDROXYALUMINUM AMINOACETATE (UNII: DO250MG0W6) KAOLIN (UNII: 24H4NWX5CO) GLYCERIN (UNII: PDC6A3C0OX) POVIDONE (UNII: FZ989GH94E) METHYLPARABEN (UNII: A2I8C7HI9T) POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) POLYSORBATE 80 (UNII: 6OZP39ZG8H) PROPYLPARABEN (UNII: Z8IX2SC1OH) POLYACRYLIC ACID (8000 MW) (UNII: 73861X4K5F) TARTARIC ACID (UNII: W4888I119H) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:67510-1301-5 1 in 1 CARTON 09/12/2011 1 5 in 1 POUCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 09/12/2011 Labeler - Kareway Product, Inc. (121840057) Establishment Name Address ID/FEI Business Operations TDS Pharm Co., Ltd. 694894612 manufacture(67510-1301)