Label: SOUTH MOON MULTI-PURPOSE NAIL SOLUTION- glycerin liquid
- NDC Code(s): 84983-008-01
- Packager: Shantou South Moon Biotechnology Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 27, 2025
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- WHEN USING
- PURPOSE
- STOP USE
- DO NOT USE
- KEEP OUT OF REACH OF CHILDREN
- STORAGE AND HANDLING
- WARNINGS
- INACTIVE INGREDIENT
- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
SOUTH MOON MULTI-PURPOSE NAIL SOLUTION
glycerin liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84983-008 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ANGELICA SINENSIS ROOT (UNII: B66F4574UG) (ANGELICA SINENSIS ROOT - UNII:B66F4574UG) ANGELICA SINENSIS ROOT 0.006 mg in 30 mg SALIX ALBA BARK (UNII: 205MXS71H7) (SALIX ALBA BARK - UNII:205MXS71H7) SALIX ALBA BARK 0.006 mg in 30 mg TEA TREE OIL (UNII: VIF565UC2G) (TEA TREE OIL - UNII:VIF565UC2G) TEA TREE OIL 0.006 mg in 30 mg Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) 27.876 mg in 30 mg GLYCERIN (UNII: PDC6A3C0OX) 0.006 mg in 30 mg SILVER CHLORIDE (UNII: MWB0804EO7) 0.6 mg in 30 mg UREA (UNII: 8W8T17847W) 1.5 mg in 30 mg Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:84983-008-01 30 mg in 1 BOTTLE; Type 0: Not a Combination Product 04/28/2025 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M016 04/28/2025 Labeler - Shantou South Moon Biotechnology Co., Ltd. (457126192) Registrant - Shantou South Moon Biotechnology Co., Ltd. (457126192) Establishment Name Address ID/FEI Business Operations Shantou South Moon Biotechnology Co., Ltd. 457126192 manufacture(84983-008)

