Label: GENITAL WARTS REMOVER CREAM (salicylic acid, chlorhexidine di- acetate ointment
- NDC Code(s): 84302-008-01
- Packager: Shenzhen Hanchuan e-commerce Co., Ltd
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated May 17, 2024
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- WARNINGS
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DOSAGE & ADMINISTRATION
After washing the fecled area with warm water,take an apropriate amount of this product with a toothpick and apply it to the surface of the aflected area. Gently knead for 5-10 minutes to make it fully absorbed. Please do not to apply it to the surrounding healthy skin andmucous membranes
2.2-3 times a day, Use it continucusly for 7 days.
If it does not fall off,it is recommended to continue to use it - INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
GENITAL WARTS REMOVER CREAM
salicylic acid, chlorhexidine di(acetate) ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84302-008 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 10 g in 100 g ACETATE ION (UNII: 569DQM74SC) (ACETATE ION - UNII:569DQM74SC) ACETATE ION 2 g in 100 g Inactive Ingredients Ingredient Name Strength BASSIA SCOPARIA WHOLE (UNII: 240G38P85Z) PINELLIA TERNATA WHOLE (UNII: 71T2LKP8GL) CHLORHEXIDINE ACETATE (UNII: 5908ZUF22Y) BRUCEA JAVANICA FRUIT (UNII: 50268139XV) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) WATER (UNII: 059QF0KO0R) PATRINIA SCABIOSIFOLIA (UNII: 3B16R130R7) ZANTHOXYLUM BUNGEANUM WHOLE (UNII: WH9894JM8K) GLYCERIN (UNII: PDC6A3C0OX) STEARIC ACID (UNII: 4ELV7Z65AP) GENTIANA LUTEA ROOT (UNII: S72O3284MS) STEMONA SESSILIFOLIA ROOT (UNII: EKG8030U4N) POTASSIUM ALUM (UNII: 1L24V9R23S) METHYLPARABEN (UNII: A2I8C7HI9T) ETHYLPARABEN (UNII: 14255EXE39) CNIDIUM MONNIERI WHOLE (UNII: GYR30735RE) BENZOIC ACID (UNII: 8SKN0B0MIM) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:84302-008-01 20 g in 1 TUBE; Type 0: Not a Combination Product 05/17/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M028 05/17/2024 Labeler - Shenzhen Hanchuan e-commerce Co., Ltd (449984812) Establishment Name Address ID/FEI Business Operations Shenzhen Hanchuan e-commerce Co., Ltd 449984812 manufacture(84302-008)