Cotton
Allergenic Extract
Approved
Approval ID
0fb71326-54c9-4139-befe-06ca832d02c8
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Dec 11, 2009
Manufacturers
FDA
Nelco Laboratories, Inc.
DUNS: 054980867
Products 9
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Jute
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code36987-2250
Application NumberBLA102192
Product Classification
M
Marketing Category
C73585
G
Generic Name
Jute
Product Specifications
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Effective DateDecember 11, 2009
FDA Product Classification
INGREDIENTS (5)
CORCORUS CAPSULARIS FIBERActive
Quantity: 0.05 g in 1 mL
Code: TVA75O7S63
Classification: ACTIB
SODIUM CHLORIDEInactive
Code: 451W47IQ8X
Classification: IACT
SODIUM BICARBONATEInactive
Code: 8MDF5V39QO
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
PHENOLInactive
Code: 339NCG44TV
Classification: IACT
Kapok
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code36987-2226
Application NumberBLA102192
Product Classification
M
Marketing Category
C73585
G
Generic Name
Kapok
Product Specifications
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Effective DateDecember 11, 2009
FDA Product Classification
INGREDIENTS (5)
WATERInactive
Code: 059QF0KO0R
Classification: IACT
PHENOLInactive
Code: 339NCG44TV
Classification: IACT
SODIUM BICARBONATEInactive
Code: 8MDF5V39QO
Classification: IACT
SODIUM CHLORIDEInactive
Code: 451W47IQ8X
Classification: IACT
CEIBA PENTANDRA FIBERActive
Quantity: 0.05 g in 1 mL
Code: 758Z9H9WV9
Classification: ACTIB
Flaxseed
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code36987-2218
Application NumberBLA102192
Product Classification
M
Marketing Category
C73585
G
Generic Name
Flaxseed
Product Specifications
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Effective DateDecember 11, 2009
FDA Product Classification
INGREDIENTS (5)
FLAX SEEDActive
Quantity: 0.05 g in 1 mL
Code: 4110YT348C
Classification: ACTIB
WATERInactive
Code: 059QF0KO0R
Classification: IACT
SODIUM BICARBONATEInactive
Code: 8MDF5V39QO
Classification: IACT
SODIUM CHLORIDEInactive
Code: 451W47IQ8X
Classification: IACT
PHENOLInactive
Code: 339NCG44TV
Classification: IACT
Tobacco Leaf
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code36987-2242
Application NumberBLA102192
Product Classification
M
Marketing Category
C73585
G
Generic Name
Tobacco Leaf
Product Specifications
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Effective DateDecember 11, 2009
FDA Product Classification
INGREDIENTS (5)
TOBACCO LEAFActive
Quantity: 0.05 g in 1 mL
Code: 6YR2608RSU
Classification: ACTIB
SODIUM CHLORIDEInactive
Code: 451W47IQ8X
Classification: IACT
SODIUM BICARBONATEInactive
Code: 8MDF5V39QO
Classification: IACT
PHENOLInactive
Code: 339NCG44TV
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
Cotton Seed
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code36987-2210
Application NumberBLA102192
Product Classification
M
Marketing Category
C73585
G
Generic Name
Cotton Seed
Product Specifications
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Effective DateDecember 11, 2009
FDA Product Classification
INGREDIENTS (5)
COTTON SEEDActive
Quantity: 0.05 g in 1 mL
Code: DI0ZRJ0MXN
Classification: ACTIB
PHENOLInactive
Code: 339NCG44TV
Classification: IACT
SODIUM CHLORIDEInactive
Code: 451W47IQ8X
Classification: IACT
SODIUM BICARBONATEInactive
Code: 8MDF5V39QO
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
Cotton
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code36987-2194
Application NumberBLA102192
Product Classification
M
Marketing Category
C73585
G
Generic Name
Cotton
Product Specifications
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Effective DateDecember 11, 2009
FDA Product Classification
INGREDIENTS (5)
COTTONActive
Quantity: 0.05 g in 1 mL
Code: 7S4U9R5259
Classification: ACTIB
PHENOLInactive
Code: 339NCG44TV
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
SODIUM BICARBONATEInactive
Code: 8MDF5V39QO
Classification: IACT
SODIUM CHLORIDEInactive
Code: 451W47IQ8X
Classification: IACT
Sisal
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code36987-2258
Application NumberBLA102192
Product Classification
M
Marketing Category
C73585
G
Generic Name
Sisal
Product Specifications
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Effective DateDecember 11, 2009
FDA Product Classification
INGREDIENTS (5)
AGAVE SISALANA FIBERActive
Quantity: 0.05 g in 1 mL
Code: MRJ91HVV4H
Classification: ACTIB
SODIUM CHLORIDEInactive
Code: 451W47IQ8X
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
SODIUM BICARBONATEInactive
Code: 8MDF5V39QO
Classification: IACT
PHENOLInactive
Code: 339NCG44TV
Classification: IACT
Cotton Linters
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code36987-2202
Application NumberBLA102192
Product Classification
M
Marketing Category
C73585
G
Generic Name
Cotton Linters
Product Specifications
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Effective DateDecember 11, 2009
FDA Product Classification
INGREDIENTS (5)
COTTON FIBERActive
Quantity: 0.05 g in 1 mL
Code: 70LDW53ROO
Classification: ACTIB
PHENOLInactive
Code: 339NCG44TV
Classification: IACT
SODIUM CHLORIDEInactive
Code: 451W47IQ8X
Classification: IACT
SODIUM BICARBONATEInactive
Code: 8MDF5V39QO
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
Orris Root
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code36987-2234
Application NumberBLA102192
Product Classification
M
Marketing Category
C73585
G
Generic Name
Orris Root
Product Specifications
Route of AdministrationINTRADERMAL, SUBCUTANEOUS
Effective DateDecember 11, 2009
FDA Product Classification
INGREDIENTS (5)
IRIS GERMANICA VAR. FLORENTINA ROOTActive
Quantity: 0.05 g in 1 mL
Code: M30XO5X4XD
Classification: ACTIB
SODIUM CHLORIDEInactive
Code: 451W47IQ8X
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
SODIUM BICARBONATEInactive
Code: 8MDF5V39QO
Classification: IACT
PHENOLInactive
Code: 339NCG44TV
Classification: IACT