- Actives
- Purpose
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Inactives
Flemingia Macrophylla Root Extract, Rubia Cordifolia Whole Root and Rhizome Extrac(12mg), Cynoglossum Lanceolatum Whole Root Extract 一(10mg), Murraya Paniculata Whole Rhizome Extract (6mg), Pittosporum Pentandrum Whole Root Extract (6mg), Sambucus Chinensis Whole Root Extract (6mg), Tanacetum Vulgare Top Root and Leaf Extract (6mg).
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Warnings
FOR EXTERNAL USE ONLY ■■ Avoid contact with eyes or mucous membranes. ■■ Do not apply to open wounds, or to damaged or irritated skin. ■■ Do not use this product if your skin is sensitive or allergic to any ingredients in this product. ■■ Discontinue use if signs of irritation or rash appear. Consult a doctor if rash worsens after removal. ■■ Avoid use on extremely hairy areas of the body to avoid discomfort when removing the patch. ■■ If pregnant or breastfeeding, consult a doctor before use. ■■ Keep out of reach of children.
- KEEP OUT OF REACH OF CHILDREN
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Directions
For adults and children 6 and older: Clean the affected area before use. Can be cut to size. Peel off film and cover affected area with patch. For menstrual pain, place on abdomen. Keep on for up to 8 hours under normal conditions. Apply once or twice per day as needed. Allow skin to breathe for a few hours between applications. Users with sensitive skin should test on a small area first.
- Indication
- Product Label
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INGREDIENTS AND APPEARANCE
PAIN RELIEF PATCHES
menthol pain relief patches patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72348-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 5 mg Inactive Ingredients Ingredient Name Strength CYNOGLOSSUM LANCEOLATUM WHOLE (UNII: F6U6XA1Z3V) FLEMINGIA MACROPHYLLA ROOT (UNII: 6U053BFF0D) TANACETUM VULGARE TOP (UNII: D52957JQ8M) MURRAYA PANICULATA WHOLE (UNII: Y8ZAA3Z7WU) RUBIA CORDIFOLIA WHOLE (UNII: 701QX6SO4L) PITTOSPORUM PENTANDRUM WHOLE (UNII: S07MT74WUF) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72348-001-01 5 in 1 BOX; Type 0: Not a Combination Product 05/16/2018 03/10/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 05/13/2018 03/10/2023 Labeler - Lhasa OMS,Inc (625752050) Establishment Name Address ID/FEI Business Operations Cheng Kuang Pharmaceutical Co., Ltd. 656281060 manufacture(72348-001)