Label: SAMSALI WART REMOVER- wart remover liquid
- NDC Code(s): 83818-002-01
- Packager: Shenzhen Xinxin Yunhai Technology Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 18, 2024
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Use
- Warnings
- Warnings
- Do not use
- When Using
- Stop Use
- Ask Doctor
- Keep Oot Of Reach Of Children
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Directions
1. Unscrew cap to open (first-time users cut thesealed round round ball at the bottle mouth with scissors).
2. Wash and dry the affected area (wart, corn, callus) before application. Squeeze bottle to evenly apply the liquid,
which dries into a film within seconds; Repeat the process for a second application.3. Immediately reseal the bottle after application to prevent air exposure as theproduct may crystallize.
4. Apply twice daily - morning and evening. Ifthe issue is foot-based, apply before bedtime to minimize friction duiring walking and enhance absorption.
5. Continue daily application for2 weeks until skin appears smooth and healthy. More severe cases may require a longer period - remain patient and consistent with the application.
- Other information
- Inactive ingredients
- Questions
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
SAMSALI WART REMOVER
wart remover liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83818-002 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 5 g in 100 mL Inactive Ingredients Ingredient Name Strength BASSIA SCOPARIA FRUIT (UNII: 04W97Z676Y) TYPHONIUM GIGANTEUM STEM (UNII: R155MDU522) DICTAMNUS DASYCARPUS ROOT BARK (UNII: LA97176ILS) GLEDITSIA SINENSIS THORN (UNII: 26LKE578NY) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:83818-002-01 20 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/17/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M028 01/17/2024 Labeler - Shenzhen Xinxin Yunhai Technology Co., Ltd. (699816806) Establishment Name Address ID/FEI Business Operations Shenzhen Xinxin Yunhai Technology Co., Ltd. 699816806 label(83818-002) , manufacture(83818-002)
