Label: SWIFTALYN WART REMOVER- wart remover liquid
- NDC Code(s): 84048-005-01
- Packager: Shenzhen Peruidaishi Technology Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated March 1, 2024
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- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Use
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Warnings
Do not use it on your face..External use only. Pregnant and breastfeeding women should be usedwith caution
* Avoid getting the product into your eyes. if it accidentally getsinto theeyes, rinse it off with water immediately..stop using and ask a physician if irritation occurs.Stop use if there is no improvement within d weeks.. keep it away from children.. it is normal for the treated wart to appear red and swollen if thishappens, stop using the product for 3-5 days Once the rednesssubsides, continue to use the product until the wart completely folls off. - Do not use
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When Using
it is normal for the treated wart to appear red and swollen. if thishappens, stop using the product for3-5 days Once the rednesssubsides, continue to use the product until the wart completely falls off.
You should begin to see the effects within 3-5 days.Typically, most minor warts take around 10 days to beremoved, while larger warts may require a longerduration for complete removal and healing - Stop Use
- Keep Oot Of Reach Of Children
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Directions
1. cleanse and dry the affected area.
2 Use the brush or cotton swab to apply the wart remaval liquid onthe wart Gently dab onto the affected area. if the wart is large, usetapping motins to cover the entire affected area.
3. Donot rub.
4. Allow 3-5 minutes for the skin to absorb it fully.
5.Apply twice a day, in the morning and evening
- Other information
- Inactive ingredients
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
SWIFTALYN WART REMOVER
wart remover liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84048-005 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 1 g in 100 mL Inactive Ingredients Ingredient Name Strength ASIATIC ACID (UNII: 9PA5A687X5) WATER (UNII: 059QF0KO0R) DEHYDRATED ALCOHOL (UNII: 3K9958V90M) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) ANGELICA DAHURICA ROOT (UNII: 1V63N2S972) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:84048-005-01 20 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/24/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M028 01/24/2024 Labeler - Shenzhen Peruidaishi Technology Co., Ltd. (706728459) Establishment Name Address ID/FEI Business Operations Shenzhen Peruidaishi Technology Co., Ltd. 706728459 label(84048-005) , manufacture(84048-005)
