Label: TOBCHARM TOENAIL FUNGUS TREATMENT LIQUID- toenail fungus treatment liquid liquid
- NDC Code(s): 85817-009-01
- Packager: Guangzhou Qiexiran Cosmetics Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 15, 2025
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Use
- Warnings
- Do not use
- When Using
- Stop Use
- Ask Doctor
- Keep Out Of Reach Of Children
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Directions
■ Before using it, clean the affected area with soap and soak the nail with warm water to soften it.
■ For toe fungus, scrape off the dirt on the nail, and gently file the thickened part of the fungal nail with a nail file until it’s flat. (be careful not to hurt the nail bed) You can use a nail file every 2-3 days to polish the surface of the affected area.
Apply the liquid with a thin layer over the affected area, the skin under the nail, and around the cuticle area.
■ For athlete’s foot, pay special attention to spaces between toes.
■ Use it twice in the morning and evening for at least 8 weeks to see the effect. And if you want complete improvement, we recommend using it for 3-6 months.
■ You can use this product preventively for fungus in hot and humid conditions. - Other information
- Inactive ingredients
- Questions
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
TOBCHARM TOENAIL FUNGUS TREATMENT LIQUID
toenail fungus treatment liquid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:85817-009 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MISOPROSTOL (UNII: 0E43V0BB57) (MISOPROSTOL - UNII:0E43V0BB57) MISOPROSTOL 10 g in 100 mL Inactive Ingredients Ingredient Name Strength PEPPERMINT OIL (UNII: AV092KU4JH) TEA TREE OIL (UNII: VIF565UC2G) APRICOT KERNEL OIL (UNII: 54JB35T06A) TOCOPHEROL (UNII: R0ZB2556P8) BERGAMOT OIL (UNII: 39W1PKE3JI) LAVENDER OIL (UNII: ZBP1YXW0H8) JOJOBA OIL (UNII: 724GKU717M) CAMPHOR OIL (UNII: 75IZZ8Y727) MINERAL OIL (UNII: T5L8T28FGP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:85817-009-01 30 mL in 1 BOTTLE; Type 0: Not a Combination Product 12/15/2025 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M005 12/15/2025 Labeler - Guangzhou Qiexiran Cosmetics Co., Ltd. (513170495) Establishment Name Address ID/FEI Business Operations Guangzhou Qiexiran Cosmetics Co., Ltd. 513170495 manufacture(85817-009)

