sunscreen
Care One 959.001 959AB Ultra Sunscreen Spray SPF 30
Approved
Approval ID
cc4d6350-9ae8-4eb6-b670-100af59f6ada
Product Type
HUMAN OTC DRUG LABEL
Effective Date
Mar 24, 2025
Manufacturers
FDA
Retail Business Services, LLC
DUNS: 967989935
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Avobenzone, Homosalate, Octisalate, Octocrylene
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code72476-959
Application NumberM020
Product Classification
M
Marketing Category
C200263
G
Generic Name
Avobenzone, Homosalate, Octisalate, Octocrylene
Product Specifications
Route of AdministrationTOPICAL
Effective DateMarch 24, 2025
FDA Product Classification
INGREDIENTS (9)
ALCOHOLInactive
Code: 3K9958V90M
Classification: IACT
BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW)Inactive
Code: JZ1374NL9E
Classification: IACT
GLYCERINInactive
Code: PDC6A3C0OX
Classification: IACT
TROLAMINEInactive
Code: 9O3K93S3TK
Classification: IACT
BUTYLOCTYL SALICYLATEInactive
Code: 2EH13UN8D3
Classification: IACT
AVOBENZONEActive
Quantity: 30 mg in 1 g
Code: G63QQF2NOX
Classification: ACTIB
HOMOSALATEActive
Quantity: 100 mg in 1 g
Code: V06SV4M95S
Classification: ACTIB
OCTISALATEActive
Quantity: 50 mg in 1 g
Code: 4X49Y0596W
Classification: ACTIB
OCTOCRYLENEActive
Quantity: 80 mg in 1 g
Code: 5A68WGF6WM
Classification: ACTIB