HYDROQUINONE
Hydroquinone USP, 4% Skin Bleaching Cream
Approved
Approval ID
a7beb629-5b90-4c4d-b31d-6dc916ed3040
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
May 6, 2020
Manufacturers
FDA
Syntenza Pharmaceuticals LLC
DUNS: 080999747
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
HYDROQUINONE
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code72056-060
Product Classification
G
Generic Name
HYDROQUINONE
Product Specifications
Route of AdministrationTOPICAL
Effective DateMay 6, 2020
FDA Product Classification
INGREDIENTS (13)
HYDROQUINONEActive
Quantity: 40 mg in 1 g
Code: XV74C1N1AE
Classification: ACTIB
WATERInactive
Code: 059QF0KO0R
Classification: IACT
Ascorbic AcidInactive
Code: PQ6CK8PD0R
Classification: IACT
GlycerinInactive
Code: PDC6A3C0OX
Classification: IACT
CETOSTEARYL ALCOHOLInactive
Code: 2DMT128M1S
Classification: IACT
LAURYL SULFATEInactive
Code: DIQ16UC154
Classification: IACT
.ALPHA.-TOCOPHEROL, DL-Inactive
Code: 7QWA1RIO01
Classification: IACT
Glycolic AcidInactive
Code: 0WT12SX38S
Classification: IACT
BISULFITE IONInactive
Code: OJ9787WBLU
Classification: IACT
MethylparabenInactive
Code: A2I8C7HI9T
Classification: IACT
EDETIC ACIDInactive
Code: 9G34HU7RV0
Classification: IACT
PropylparabenInactive
Code: Z8IX2SC1OH
Classification: IACT
Butylated HydroxytolueneInactive
Code: 1P9D0Z171K
Classification: IACT