Label: SKAPEMED SKIN REPAIR- tolnaftate 1% skin repair liquid
- NDC Code(s): 84010-035-01
- Packager: Jiangxi Hemei Pharmaceutical Co., Ltd
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 8, 2024
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- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Use
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Warnings
For external use only
Extremely Flammable do not use while smoking or near heat or flame. Do not use on children under 2 years of age unless directed by a doctor.When using this product avoid contact with the eyes·Use only as directed.Intentional misuse by deliberately concentrating and inhaling the contents can be harmful or fatal .Do not puncture orincinerate. Contents under pressure. Do not store attemperatures above 120°F
- Do not use
- When Using
- Stop Use
- Ask Doctor
- Keep Oot Of Reach Of Children
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Directions
·Wash the affected area and dry thoroughly
·Shake the can well. Apply a thin layer on the affected area twice a day (in the morning and at night). ·Supervise children in the use of this product
·Use daily for 4 weeks; if condition persists longer, ask a doctor
·This product is not effective on the scalp or nails.
- Other information
- Inactive ingredients
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
SKAPEMED SKIN REPAIR
tolnaftate 1% skin repair liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84010-035 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TOLNAFTATE (UNII: 06KB629TKV) (TOLNAFTATE - UNII:06KB629TKV) TOLNAFTATE 1 g in 100 mL Inactive Ingredients Ingredient Name Strength BENZOIC ACID (UNII: 8SKN0B0MIM) PHELLODENDRON AMURENSE BARK (UNII: PBG27B754G) PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) PSEUDOLARIX AMABILIS BARK (UNII: 49G13A93VE) SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K) EUPHORBIA HIRTA WHOLE (UNII: L13YF113GN) NIACINAMIDE (UNII: 25X51I8RD4) VITAMIN A (UNII: 81G40H8B0T) SALICYLIC ACID (UNII: O414PZ4LPZ) LACTIC ACID (UNII: 33X04XA5AT) ALCOHOL (UNII: 3K9958V90M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:84010-035-01 50 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/09/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M005 10/09/2024 Labeler - Jiangxi Hemei Pharmaceutical Co., Ltd (724892056) Establishment Name Address ID/FEI Business Operations Jiangxi Hemei Pharmaceutical Co., Ltd 724892056 manufacture(84010-035)