MedPath

EELHOE Bio Sun Stick

Approved
Approval ID

349a3d72-9969-855d-e063-6394a90a281c

Product Type

HUMAN OTC DRUG LABEL

Effective Date

May 8, 2025

Manufacturers
FDA

Shantou Eelhoe Daily Chemical Technology Co., Ltd.

DUNS: 617290813

Products 1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

TITANIUM DIOXIDE

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code85064-008
Application NumberM020
Product Classification
M
Marketing Category
C200263
G
Generic Name
TITANIUM DIOXIDE
Product Specifications
Route of AdministrationTOPICAL
Effective DateMay 8, 2025
FDA Product Classification

INGREDIENTS (7)

CAMELLIA JAPONICA FLOWERActive
Quantity: 0.03 mg in 15 mg
Code: KUB8101TNF
Classification: ACTIB
ISONONYL ISONONANOATEInactive
Quantity: 0.6 mg in 15 mg
Code: S4V5BS6GCX
Classification: IACT
AQUAInactive
Quantity: 13.335 mg in 15 mg
Code: 059QF0KO0R
Classification: IACT
ARTEMISIA VULGARIS ROOTActive
Quantity: 0.03 mg in 15 mg
Code: 32MP823R8S
Classification: ACTIB
GLYCERYL STEARATEInactive
Quantity: 0.225 mg in 15 mg
Code: 230OU9XXE4
Classification: IACT
ETHYLHEXYL METHOXYCINNAMATEInactive
Quantity: 0.75 mg in 15 mg
Code: 4Y5P7MUD51
Classification: IACT
TITANIUM DIOXIDEInactive
Quantity: 0.03 mg in 15 mg
Code: 15FIX9V2JP
Classification: IACT

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