MedPath

Carp

Allergenic Extract

Approved
Approval ID

026f2f1e-71cf-47ab-a24d-66663ff98429

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Dec 10, 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.

Smelt

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code36987-1265
Application NumberBLA102192
Product Classification
M
Marketing Category
C73585
G
Generic Name
Smelt
Product Specifications
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Effective DateDecember 10, 2009
FDA Product Classification

INGREDIENTS (6)

SODIUM BICARBONATEInactive
Code: 8MDF5V39QO
Classification: IACT
SODIUM CHLORIDEInactive
Code: 451W47IQ8X
Classification: IACT
SMELTActive
Quantity: 0.1 g in 1 mL
Code: 9VVF5SCM9I
Classification: ACTIB
PHENOLInactive
Code: 339NCG44TV
Classification: IACT
GLYCERINInactive
Code: PDC6A3C0OX
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT

Pike

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code36987-1241
Application NumberBLA102192
Product Classification
M
Marketing Category
C73585
G
Generic Name
Pike
Product Specifications
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Effective DateDecember 10, 2009
FDA Product Classification

INGREDIENTS (6)

NORTHERN PIKEActive
Quantity: 0.1 g in 1 mL
Code: 5JKY494U4L
Classification: ACTIB
SODIUM CHLORIDEInactive
Code: 451W47IQ8X
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
SODIUM BICARBONATEInactive
Code: 8MDF5V39QO
Classification: IACT
PHENOLInactive
Code: 339NCG44TV
Classification: IACT
GLYCERINInactive
Code: PDC6A3C0OX
Classification: IACT

Tuna Fish

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code36987-1277
Application NumberBLA102192
Product Classification
M
Marketing Category
C73585
G
Generic Name
Tuna Fish
Product Specifications
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Effective DateDecember 10, 2009
FDA Product Classification

INGREDIENTS (6)

SODIUM BICARBONATEInactive
Code: 8MDF5V39QO
Classification: IACT
SODIUM CHLORIDEInactive
Code: 451W47IQ8X
Classification: IACT
TUNAActive
Quantity: 0.1 g in 1 mL
Code: V2T3IHT3E2
Classification: ACTIB
PHENOLInactive
Code: 339NCG44TV
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
GLYCERINInactive
Code: PDC6A3C0OX
Classification: IACT

Haddock

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code36987-1217
Application NumberBLA102192
Product Classification
M
Marketing Category
C73585
G
Generic Name
Haddock
Product Specifications
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Effective DateDecember 10, 2009
FDA Product Classification

INGREDIENTS (6)

SODIUM CHLORIDEInactive
Code: 451W47IQ8X
Classification: IACT
HADDOCKActive
Quantity: 0.1 g in 1 mL
Code: 0WLY635722
Classification: ACTIB
SODIUM BICARBONATEInactive
Code: 8MDF5V39QO
Classification: IACT
PHENOLInactive
Code: 339NCG44TV
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
GLYCERINInactive
Code: PDC6A3C0OX
Classification: IACT

Salmon

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code36987-1249
Application NumberBLA102192
Product Classification
M
Marketing Category
C73585
G
Generic Name
Salmon
Product Specifications
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Effective DateDecember 10, 2009
FDA Product Classification

INGREDIENTS (6)

ATLANTIC SALMONActive
Quantity: 0.1 g in 1 mL
Code: 7062I37LB3
Classification: ACTIB
SODIUM BICARBONATEInactive
Code: 8MDF5V39QO
Classification: IACT
SODIUM CHLORIDEInactive
Code: 451W47IQ8X
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
GLYCERINInactive
Code: PDC6A3C0OX
Classification: IACT
PHENOLInactive
Code: 339NCG44TV
Classification: IACT

Shrimp

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code36987-1261
Application NumberBLA102192
Product Classification
M
Marketing Category
C73585
G
Generic Name
Shrimp
Product Specifications
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Effective DateDecember 10, 2009
FDA Product Classification

INGREDIENTS (6)

SHRIMPActive
Quantity: 0.1 g in 1 mL
Code: 1891LE191T
Classification: ACTIB
SODIUM CHLORIDEInactive
Code: 451W47IQ8X
Classification: IACT
PHENOLInactive
Code: 339NCG44TV
Classification: IACT
SODIUM BICARBONATEInactive
Code: 8MDF5V39QO
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
GLYCERINInactive
Code: PDC6A3C0OX
Classification: IACT

Scallop

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code36987-1257
Application NumberBLA102192
Product Classification
M
Marketing Category
C73585
G
Generic Name
Scallop
Product Specifications
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Effective DateDecember 10, 2009
FDA Product Classification

INGREDIENTS (6)

SCALLOPActive
Quantity: 0.1 g in 1 mL
Code: D380C73WOU
Classification: ACTIB
SODIUM CHLORIDEInactive
Code: 451W47IQ8X
Classification: IACT
PHENOLInactive
Code: 339NCG44TV
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
SODIUM BICARBONATEInactive
Code: 8MDF5V39QO
Classification: IACT
GLYCERINInactive
Code: PDC6A3C0OX
Classification: IACT

Oyster

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code36987-1237
Application NumberBLA102192
Product Classification
M
Marketing Category
C73585
G
Generic Name
Oyster
Product Specifications
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Effective DateDecember 10, 2009
FDA Product Classification

INGREDIENTS (6)

OYSTERActive
Quantity: 0.1 g in 1 mL
Code: S614XWR17V
Classification: ACTIB
SODIUM CHLORIDEInactive
Code: 451W47IQ8X
Classification: IACT
SODIUM BICARBONATEInactive
Code: 8MDF5V39QO
Classification: IACT
PHENOLInactive
Code: 339NCG44TV
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
GLYCERINInactive
Code: PDC6A3C0OX
Classification: IACT

Sword Fish

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code36987-1269
Application NumberBLA102192
Product Classification
M
Marketing Category
C73585
G
Generic Name
Sword Fish
Product Specifications
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Effective DateDecember 10, 2009
FDA Product Classification

INGREDIENTS (6)

SWORDFISHActive
Quantity: 0.1 g in 1 mL
Code: 01695YPV36
Classification: ACTIB
SODIUM CHLORIDEInactive
Code: 451W47IQ8X
Classification: IACT
SODIUM BICARBONATEInactive
Code: 8MDF5V39QO
Classification: IACT
PHENOLInactive
Code: 339NCG44TV
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
GLYCERINInactive
Code: PDC6A3C0OX
Classification: IACT

Mackerel

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code36987-1233
Application NumberBLA102192
Product Classification
M
Marketing Category
C73585
G
Generic Name
Mackerel
Product Specifications
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Effective DateDecember 10, 2009
FDA Product Classification

INGREDIENTS (6)

MACKERELActive
Quantity: 0.1 g in 1 mL
Code: CYO6K3VM7F
Classification: ACTIB
SODIUM BICARBONATEInactive
Code: 8MDF5V39QO
Classification: IACT
SODIUM CHLORIDEInactive
Code: 451W47IQ8X
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
PHENOLInactive
Code: 339NCG44TV
Classification: IACT
GLYCERINInactive
Code: PDC6A3C0OX
Classification: IACT

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