Scartrate Cream
Scartrate Cream
Approved
Approval ID
1d666463-8294-5f78-e063-6294a90a91a7
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
May 7, 2025
Manufacturers
FDA
Puretek Corporation
DUNS: 785961046
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Dimethicone, Allantoin
PRODUCT DETAILS
NDC Product Code59088-326
Application NumberN/A
Marketing CategoryN/A
Route of AdministrationTOPICAL
Effective DateMay 7, 2025
Generic NameDimethicone, Allantoin
INGREDIENTS (18)
.ALPHA.-TOCOPHEROL ACETATEInactive
Code: 9E8X80D2L0
Classification: IACT
PHENOXYETHANOLInactive
Code: HIE492ZZ3T
Classification: IACT
GLYCERINInactive
Code: PDC6A3C0OX
Classification: IACT
EDETATE DISODIUMInactive
Code: 7FLD91C86K
Classification: IACT
KUKUI NUT OILInactive
Code: TP11QR7B8R
Classification: IACT
BUTYLENE GLYCOLInactive
Code: 3XUS85K0RA
Classification: IACT
MARINE COLLAGEN, SOLUBLEInactive
Code: 8JC99XGU4W
Classification: IACT
SAFFLOWER OILInactive
Code: 65UEH262IS
Classification: IACT
GLYCERYL 1-STEARATEInactive
Code: 258491E1RZ
Classification: IACT
PEG-100 STEARATEInactive
Code: YD01N1999R
Classification: IACT
STEARIC ACIDInactive
Code: 4ELV7Z65AP
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
ALOE VERA LEAFInactive
Code: ZY81Z83H0X
Classification: IACT
DIMETHICONEActive
Quantity: 50 mg in 1 g
Code: 92RU3N3Y1O
Classification: ACTIB
CETYL ALCOHOLInactive
Code: 936JST6JCN
Classification: IACT
SODIUM HYDROXIDEInactive
Code: 55X04QC32I
Classification: IACT
DIMETHICONE CROSSPOLYMERInactive
Code: UF7620L1W6
Classification: IACT
ALLANTOINActive
Quantity: 22.5 mg in 1 g
Code: 344S277G0Z
Classification: ACTIB