Sepia
DRUG FACTS:
Approved
Approval ID
02506ea3-276b-452e-8477-ca49b329a3b8
Product Type
HUMAN OTC DRUG LABEL
Effective Date
Apr 29, 2025
Manufacturers
FDA
Energique, Inc.
DUNS: 789886132
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Sepia
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code44911-0391
Product Classification
G
Generic Name
Sepia
Product Specifications
Route of AdministrationORAL
Effective DateApril 29, 2025
FDA Product Classification
INGREDIENTS (3)
WATERInactive
Code: 059QF0KO0R
Classification: IACT
ALCOHOLInactive
Code: 3K9958V90M
Classification: IACT
SEPIA OFFICINALIS JUICEActive
Quantity: 200 [hp_C] in 1 mL
Code: QDL83WN8C2
Classification: ACTIB