Acacia
Allergenic Extract
Approved
Approval ID
de47ad70-b2be-4103-a402-35463ebffc87
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Dec 3, 2009
Manufacturers
FDA
Nelco Laboratories, Inc.
DUNS: 054980867
Products 10
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Balsam Poplar
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code36987-3119
Application NumberBLA102192
Product Classification
M
Marketing Category
C73585
G
Generic Name
Balsam Poplar
Product Specifications
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Effective DateDecember 3, 2009
FDA Product Classification
INGREDIENTS (5)
SODIUM CHLORIDEInactive
Code: 451W47IQ8X
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
POPULUS BALSAMIFERA SUBSP. TRICHOCARPA POLLENActive
Quantity: 20000 [PNU] in 1 mL
Code: H8QYU50Z2D
Classification: ACTIB
SODIUM BICARBONATEInactive
Code: 8MDF5V39QO
Classification: IACT
PHENOLInactive
Code: 339NCG44TV
Classification: IACT
Poplar
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code36987-3111
Application NumberBLA102192
Product Classification
M
Marketing Category
C73585
G
Generic Name
Poplar
Product Specifications
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Effective DateDecember 3, 2009
FDA Product Classification
INGREDIENTS (5)
POPULUS DELTOIDES POLLENActive
Quantity: 20000 [PNU] in 1 mL
Code: 476DVV63WP
Classification: ACTIB
SODIUM CHLORIDEInactive
Code: 451W47IQ8X
Classification: IACT
SODIUM BICARBONATEInactive
Code: 8MDF5V39QO
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
PHENOLInactive
Code: 339NCG44TV
Classification: IACT
Black Willow
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code36987-3087
Application NumberBLA102192
Product Classification
M
Marketing Category
C73585
G
Generic Name
Black Willow
Product Specifications
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Effective DateDecember 3, 2009
FDA Product Classification
INGREDIENTS (5)
SALIX NIGRA POLLENActive
Quantity: 20000 [PNU] in 1 mL
Code: 6M2JIH93ZN
Classification: ACTIB
WATERInactive
Code: 059QF0KO0R
Classification: IACT
SODIUM CHLORIDEInactive
Code: 451W47IQ8X
Classification: IACT
SODIUM BICARBONATEInactive
Code: 8MDF5V39QO
Classification: IACT
PHENOLInactive
Code: 339NCG44TV
Classification: IACT
English Walnut
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code36987-3079
Application NumberBLA102192
Product Classification
M
Marketing Category
C73585
G
Generic Name
English Walnut
Product Specifications
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Effective DateDecember 3, 2009
FDA Product Classification
INGREDIENTS (5)
JUGLANS REGIA POLLENActive
Quantity: 20000 [PNU] in 1 mL
Code: ARW43087I1
Classification: ACTIB
SODIUM BICARBONATEInactive
Code: 8MDF5V39QO
Classification: IACT
SODIUM CHLORIDEInactive
Code: 451W47IQ8X
Classification: IACT
PHENOLInactive
Code: 339NCG44TV
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
Black Walnut
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code36987-3063
Application NumberBLA102192
Product Classification
M
Marketing Category
C73585
G
Generic Name
Black Walnut
Product Specifications
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Effective DateDecember 3, 2009
FDA Product Classification
INGREDIENTS (5)
SODIUM BICARBONATEInactive
Code: 8MDF5V39QO
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
PHENOLInactive
Code: 339NCG44TV
Classification: IACT
JUGLANS NIGRA POLLENActive
Quantity: 20000 [PNU] in 1 mL
Code: 1BV28146ZR
Classification: ACTIB
SODIUM CHLORIDEInactive
Code: 451W47IQ8X
Classification: IACT
Pussy Willow
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code36987-3103
Application NumberBLA102192
Product Classification
M
Marketing Category
C73585
G
Generic Name
Pussy Willow
Product Specifications
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Effective DateDecember 3, 2009
FDA Product Classification
INGREDIENTS (5)
SODIUM BICARBONATEInactive
Code: 8MDF5V39QO
Classification: IACT
PHENOLInactive
Code: 339NCG44TV
Classification: IACT
SALIX DISCOLOR POLLENActive
Quantity: 20000 [PNU] in 1 mL
Code: ER172J09FM
Classification: ACTIB
SODIUM CHLORIDEInactive
Code: 451W47IQ8X
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
Arroyo Willow
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code36987-3095
Application NumberBLA102192
Product Classification
M
Marketing Category
C73585
G
Generic Name
Arroyo Willow
Product Specifications
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Effective DateDecember 3, 2009
FDA Product Classification
INGREDIENTS (5)
SODIUM BICARBONATEInactive
Code: 8MDF5V39QO
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
SALIX LASIOLEPIS POLLENActive
Quantity: 20000 [PNU] in 1 mL
Code: 808UWJ59FI
Classification: ACTIB
SODIUM CHLORIDEInactive
Code: 451W47IQ8X
Classification: IACT
PHENOLInactive
Code: 339NCG44TV
Classification: IACT
Privet
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code36987-3023
Application NumberBLA102192
Product Classification
M
Marketing Category
C73585
G
Generic Name
Privet
Product Specifications
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Effective DateDecember 3, 2009
FDA Product Classification
INGREDIENTS (5)
LIGUSTRUM VULGARE POLLENActive
Quantity: 20000 [PNU] in 1 mL
Code: Y3FRX92Z0E
Classification: ACTIB
SODIUM CHLORIDEInactive
Code: 451W47IQ8X
Classification: IACT
PHENOLInactive
Code: 339NCG44TV
Classification: IACT
SODIUM BICARBONATEInactive
Code: 8MDF5V39QO
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
Lombardy Poplar
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code36987-3007
Application NumberBLA102192
Product Classification
M
Marketing Category
C73585
G
Generic Name
Lombardy Poplar
Product Specifications
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Effective DateDecember 3, 2009
FDA Product Classification
INGREDIENTS (5)
POPULUS NIGRA POLLENActive
Quantity: 20000 [PNU] in 1 mL
Code: 0MGE63QPFJ
Classification: ACTIB
PHENOLInactive
Code: 339NCG44TV
Classification: IACT
SODIUM BICARBONATEInactive
Code: 8MDF5V39QO
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
SODIUM CHLORIDEInactive
Code: 451W47IQ8X
Classification: IACT
Slash Pine
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code36987-2967
Application NumberBLA102192
Product Classification
M
Marketing Category
C73585
G
Generic Name
Slash Pine
Product Specifications
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Effective DateDecember 3, 2009
FDA Product Classification
INGREDIENTS (5)
SODIUM CHLORIDEInactive
Code: 451W47IQ8X
Classification: IACT
SODIUM BICARBONATEInactive
Code: 8MDF5V39QO
Classification: IACT
PINUS ELLIOTTII POLLENActive
Quantity: 20000 [PNU] in 1 mL
Code: QJB9OQO689
Classification: ACTIB
WATERInactive
Code: 059QF0KO0R
Classification: IACT
PHENOLInactive
Code: 339NCG44TV
Classification: IACT