Label: NAIL FUNGUS TREATMENT- tomumia nail fungus liquid
- NDC Code(s): 83299-030-01
- Packager: Consilii LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated June 13, 2024
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- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
-
Use
(Usage)
Clean the affected area with soap and warm water and dry thoroughly.
Gently file thickened part of the fungal nail with a nail file until it's flat.
Using the brush, apply a thin layer of liquid onto the affected area.
Repeat this process 2 times daily for
1-2 weeks (or) until the infection is gone - Warnings
- Do not use
- When Using
- Stop Use
- Ask Doctor
- Keep Oot Of Reach Of Children
-
Directions
1. For thickened and hard nails, itmust be thinned before use.
2.lf there is a slight deposit, it is thechinese medicinal material, feel
free to use it.3. After healthy nails grow, takecare and do not file them. Alwayskeep the hands and feet clean,After the nails are normal, continue
to use for 30 days. - Other information
- Inactive ingredients
- Questions
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
NAIL FUNGUS TREATMENT
tomumia nail fungus liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83299-030 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CHLORHEXIDINE ACETATE (UNII: 5908ZUF22Y) (CHLORHEXIDINE - UNII:R4KO0DY52L) CHLORHEXIDINE ACETATE 0.3 g in 100 mL Inactive Ingredients Ingredient Name Strength ANGELICA DAHURICA SEED (UNII: 9M69B50875) CHLORHEXIDINE (UNII: R4KO0DY52L) ILEX CORNUTA WHOLE (UNII: 9WEY0RQ9HO) VITEXIN (UNII: 9VP70K75OK) SOPHORA FLAVESCENS WHOLE (UNII: X8KX602M5L) IMPATIENS WALLERIANA WHOLE (UNII: 8W4759RC84) ACETATE ION (UNII: 569DQM74SC) STEMONA TUBEROSA WHOLE (UNII: 9373ZOT316) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:83299-030-01 30 mL in 1 BOTTLE; Type 0: Not a Combination Product 06/13/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M005 06/13/2024 Labeler - Consilii LLC (118891890) Establishment Name Address ID/FEI Business Operations Consilii LLC 118891890 label(83299-030) , manufacture(83299-030)