California Mugwort
Allergenic Extract
Approved
Approval ID
02de3b96-7daa-4776-8e2e-c21cf282f091
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Dec 4, 2009
Manufacturers
FDA
Nelco Laboratories, Inc.
DUNS: 054980867
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
California Mugwort
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code36987-3283
Application NumberBLA102192
Product Classification
M
Marketing Category
C73585
G
Generic Name
California Mugwort
Product Specifications
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Effective DateDecember 4, 2009
FDA Product Classification
INGREDIENTS (6)
SODIUM CHLORIDEInactive
Code: 451W47IQ8X
Classification: IACT
SODIUM BICARBONATEInactive
Code: 8MDF5V39QO
Classification: IACT
ARTEMISIA DOUGLASIANA POLLENActive
Quantity: 0.05 g in 1 mL
Code: K1301R7883
Classification: ACTIB
PHENOLInactive
Code: 339NCG44TV
Classification: IACT
GLYCERINInactive
Code: PDC6A3C0OX
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT