SOUTH MOON Multi-Purpose Nail Solution
Approved
Approval ID
33d25de4-4f99-1a9e-e063-6394a90a15c4
Product Type
HUMAN OTC DRUG LABEL
Effective Date
Apr 28, 2025
Manufacturers
FDA
Shantou South Moon Biotechnology Co., Ltd.
DUNS: 457126192
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
GLYCERIN
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code84983-008
Application NumberM016
Product Classification
M
Marketing Category
C200263
G
Generic Name
GLYCERIN
Product Specifications
Route of AdministrationTOPICAL
Effective DateApril 28, 2025
FDA Product Classification
INGREDIENTS (7)
WATERInactive
Quantity: 27.876 mg in 30 mg
Code: 059QF0KO0R
Classification: IACT
GLYCERINInactive
Quantity: 0.006 mg in 30 mg
Code: PDC6A3C0OX
Classification: IACT
ANGELICA SINENSIS ROOTActive
Quantity: 0.006 mg in 30 mg
Code: B66F4574UG
Classification: ACTIB
SALIX ALBA BARKActive
Quantity: 0.006 mg in 30 mg
Code: 205MXS71H7
Classification: ACTIB
SILVER CHLORIDEInactive
Quantity: 0.6 mg in 30 mg
Code: MWB0804EO7
Classification: IACT
TEA TREE OILActive
Quantity: 0.006 mg in 30 mg
Code: VIF565UC2G
Classification: ACTIB
UREAInactive
Quantity: 1.5 mg in 30 mg
Code: 8W8T17847W
Classification: IACT