Label: K-POWER PATCH- achyranthes bidentata extract, achyranthes bidentata extract, patch
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Contains inactivated NDC Code(s)
NDC Code(s): 83404-301-01 - Packager: BCT
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated April 13, 2023
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- Active Ingredients
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Purposes
Achyranthes bidentata Extract 3% --------------------------Topical analgesic
Lithospermum erythrorhizon S.et Z Extract 3% -----------Topical analgesic
Xanthium strumarium L Extract 2% -------------------------Topical analgesic
Eucomniia ulmoides Extract 2% ----------------------------Topical analgesic
Harpagophytum prostrate 1% --------------------------------Topical analgesic
Capsaicin 0.4% ----------------------------------------------- Topical analgesic - Uses
- Warnings
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- Directions
- Inactive Ingredients
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INGREDIENTS AND APPEARANCE
K-POWER PATCH
achyranthes bidentata extract, achyranthes bidentata extract, patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83404-301 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LITHOSPERMUM ERYTHRORHIZON WHOLE (UNII: Y4JMM1JAWJ) (LITHOSPERMUM ERYTHRORHIZON WHOLE - UNII:Y4JMM1JAWJ) LITHOSPERMUM ERYTHRORHIZON WHOLE 3 g in 100 mm CAPSAICIN (UNII: S07O44R1ZM) (CAPSAICIN - UNII:S07O44R1ZM) CAPSAICIN 0.4 g in 100 mm XANTHIUM STRUMARIUM LEAF (UNII: AW4S0K7ELS) (XANTHIUM STRUMARIUM LEAF - UNII:AW4S0K7ELS) XANTHIUM STRUMARIUM LEAF 2 g in 100 mm EUCOMMIA ULMOIDES WHOLE (UNII: 21176878UY) (EUCOMMIA ULMOIDES WHOLE - UNII:21176878UY) EUCOMMIA ULMOIDES WHOLE 2 g in 100 mm HARPAGOPHYTUM PROCUMBENS WHOLE (UNII: BY51E8JN4B) (HARPAGOPHYTUM PROCUMBENS WHOLE - UNII:BY51E8JN4B) HARPAGOPHYTUM PROCUMBENS WHOLE 1 g in 100 mm ACHYRANTHES BIDENTATA WHOLE (UNII: 0B5LIZ2V2H) (ACHYRANTHES BIDENTATA WHOLE - UNII:0B5LIZ2V2H) ACHYRANTHES BIDENTATA WHOLE 3 g in 100 mm Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) DISODIUM DECYL PHENYL ETHER DISULFONATE (UNII: 57S4ZXM7XU) BUTYL ACRYLATE/METHYL METHACRYLATE/PERFLUOROHEXYLETHYL METHACRYLATE COPOLYMER (SALUS AF) (UNII: HLB263IJK9) SCHORL TOURMALINE (UNII: 173O8XLY6T) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:83404-301-01 85 mm in 1 PATCH; Type 0: Not a Combination Product 05/30/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 05/30/2023 Labeler - BCT (695661890) Registrant - BCT (695661890) Establishment Name Address ID/FEI Business Operations BCT 695661890 manufacture(83404-301)