Selenium Sulfide
Selenium Sulfide
Approved
Approval ID
c25a6d26-6ca8-4b85-a1c5-cc0b538744a5
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Mar 1, 2023
Manufacturers
FDA
Bryant Ranch Prepack
DUNS: 171714327
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
selenium sulfide
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code63629-1149
Product Classification
G
Generic Name
selenium sulfide
Product Specifications
Route of AdministrationTOPICAL
Effective DateOctober 3, 2020
FDA Product Classification
INGREDIENTS (14)
AMMONIUM LAURYL SULFATEInactive
Code: Q7AO2R1M0B
Classification: IACT
COCAMIDOPROPYL BETAINEInactive
Code: 5OCF3O11KX
Classification: IACT
EDETIC ACIDInactive
Code: 9G34HU7RV0
Classification: IACT
.ALPHA.-TOCOPHEROL ACETATEInactive
Code: 9E8X80D2L0
Classification: IACT
FD&C RED NO. 40Inactive
Code: WZB9127XOA
Classification: IACT
METHYLPARABENInactive
Code: A2I8C7HI9T
Classification: IACT
D&C YELLOW NO. 10Inactive
Code: 35SW5USQ3G
Classification: IACT
PANTHENOLInactive
Code: WV9CM0O67Z
Classification: IACT
PROPYLPARABENInactive
Code: Z8IX2SC1OH
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
XANTHAN GUMInactive
Code: TTV12P4NEE
Classification: IACT
PYRITHIONE ZINCInactive
Code: R953O2RHZ5
Classification: IACT
UREAInactive
Code: 8W8T17847W
Classification: IACT
SELENIUM SULFIDEActive
Quantity: 23 mg in 1 mL
Code: Z69D9E381Q
Classification: ACTIB