NDC 36987-3448 Wormwood

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
36987-3448
Proprietary Name:
Wormwood
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Nelco Laboratories, Inc.
Labeler Code:
36987
Start Marketing Date: [9]
08-29-1972
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 36987-3448-1

Package Description: 5 mL in 1 VIAL, MULTI-DOSE

NDC Code 36987-3448-2

Package Description: 10 mL in 1 VIAL, MULTI-DOSE

NDC Code 36987-3448-3

Package Description: 30 mL in 1 VIAL, MULTI-DOSE

NDC Code 36987-3448-4

Package Description: 50 mL in 1 VIAL, MULTI-DOSE

Product Details

What is NDC 36987-3448?

The NDC code 36987-3448 is assigned by the FDA to the product Wormwood which is product labeled by Nelco Laboratories, Inc.. The product's dosage form is . The product is distributed in 4 packages with assigned NDC codes 36987-3448-1 5 ml in 1 vial, multi-dose , 36987-3448-2 10 ml in 1 vial, multi-dose , 36987-3448-3 30 ml in 1 vial, multi-dose , 36987-3448-4 50 ml in 1 vial, multi-dose . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Wormwood?

Allergenic extracts are indicated for use in diagnostic testing and as part of a treatment regime for allergic disease, as established by allergy history and skin test reactivity. Allergenic extracts are indicated for the treatment of allergen specific allergic disease for use as hyposensitization or immunotherapy when avoidance of specific allergens can not be attained. The use of allergenic extracts for therapeutic purpose has been established by well-controlled clinical studies. Allergenic extracts may be used as adjunctive therapy along with pharmacotherapy which includes antihistamines, corticosteroids, and cromoglycate, and avoidance measures. Allergenic extracts for therapeutic use should be given using only the allergen selection to which the patient is allergic, has a history of exposure and are likely to be exposed to again.

Which are Wormwood UNII Codes?

The UNII codes for the active ingredients in this product are:

  • TARAXACUM OFFICINALE POLLEN (UNII: WQ3S5294XY)
  • TARAXACUM OFFICINALE POLLEN (UNII: WQ3S5294XY) (Active Moiety)
  • ATRIPLEX POLYCARPA POLLEN (UNII: JQ87AA60GU)
  • ATRIPLEX POLYCARPA POLLEN (UNII: JQ87AA60GU) (Active Moiety)
  • BACCHARIS HALIMIFOLIA POLLEN (UNII: BBO1IJ3ZIW)
  • BACCHARIS HALIMIFOLIA POLLEN (UNII: BBO1IJ3ZIW) (Active Moiety)
  • HYMENOCLEA SALSOLA POLLEN (UNII: 662J7FTA7T)
  • HYMENOCLEA SALSOLA POLLEN (UNII: 662J7FTA7T) (Active Moiety)
  • XANTHIUM STRUMARIUM POLLEN (UNII: 2QOF601J1M)
  • XANTHIUM STRUMARIUM POLLEN (UNII: 2QOF601J1M) (Active Moiety)
  • RUMEX CRISPUS POLLEN (UNII: V825XJG64G)
  • RUMEX CRISPUS (UNII: S9T422Q956) (Active Moiety)
  • EUPATORIUM CAPILLIFOLIUM POLLEN (UNII: B67NF86HF0)
  • EUPATORIUM CAPILLIFOLIUM POLLEN (UNII: B67NF86HF0) (Active Moiety)
  • KOCHIA SCOPARIA POLLEN (UNII: 07A108ZKW5)
  • KOCHIA SCOPARIA POLLEN (UNII: 07A108ZKW5) (Active Moiety)
  • SOLIDAGO CANADENSIS POLLEN (UNII: 644CZ16IR5)
  • SOLIDAGO CANADENSIS POLLEN (UNII: 644CZ16IR5) (Active Moiety)
  • AMARANTHUS TUBERCULATUS POLLEN (UNII: 92N6W6KO2G)
  • AMARANTHUS TUBERCULATUS POLLEN (UNII: 92N6W6KO2G) (Active Moiety)
  • ALLENROLFEA OCCIDENTALIS POLLEN (UNII: 5W6JAI84OI)
  • ALLENROLFEA OCCIDENTALIS POLLEN (UNII: 5W6JAI84OI) (Active Moiety)
  • CHENOPODIUM ALBUM POLLEN (UNII: 098LKX5NCN)
  • CHENOPODIUM ALBUM POLLEN (UNII: 098LKX5NCN) (Active Moiety)
  • ATRIPLEX LENTIFORMIS POLLEN (UNII: 86LWA5503I)
  • ATRIPLEX LENTIFORMIS POLLEN (UNII: 86LWA5503I) (Active Moiety)
  • IVA XANTHIFOLIA POLLEN (UNII: V80TPZ0T6J)
  • IVA ANGUSTIFOLIA POLLEN (UNII: UBW6O1H50I) (Active Moiety)
  • IVA ANNUA VAR. ANNUA POLLEN (UNII: Y2U5S5PF22)
  • IVA ANNUA VAR. ANNUA POLLEN (UNII: Y2U5S5PF22) (Active Moiety)
  • CHENOPODIUM AMBROSIOIDES POLLEN (UNII: WIB701MW2H)
  • CHENOPODIUM AMBROSIOIDES POLLEN (UNII: WIB701MW2H) (Active Moiety)
  • ARTEMISIA VULGARIS POLLEN (UNII: ANT994T71D)
  • ARTEMISIA VULGARIS POLLEN (UNII: ANT994T71D) (Active Moiety)
  • ARTEMISIA LUDOVICIANA POLLEN (UNII: 57KIJ4772H)
  • ARTEMISIA LUDOVICIANA POLLEN (UNII: 57KIJ4772H) (Active Moiety)
  • URTICA DIOICA POLLEN (UNII: DNB59M1NVU)
  • URTICA DIOICA POLLEN (UNII: DNB59M1NVU) (Active Moiety)
  • AMARANTHUS PALMERI POLLEN (UNII: 1GH3WV23KH)
  • AMARANTHUS PALMERI POLLEN (UNII: 1GH3WV23KH) (Active Moiety)
  • AMARANTHUS RETROFLEXUS POLLEN (UNII: 73B14PX5FW)
  • AMARANTHUS RETROFLEXUS POLLEN (UNII: 73B14PX5FW) (Active Moiety)
  • AMARANTHUS SPINOSUS POLLEN (UNII: 380W4HYR6N)
  • AMARANTHUS SPINOSUS POLLEN (UNII: 380W4HYR6N) (Active Moiety)
  • PLANTAGO LANCEOLATA POLLEN (UNII: DO87T1U2CI)
  • PLANTAGO LANCEOLATA POLLEN (UNII: DO87T1U2CI) (Active Moiety)
  • IVA AXILLARIS POLLEN (UNII: 13KFG30UBR)
  • IVA AXILLARIS POLLEN (UNII: 13KFG30UBR) (Active Moiety)
  • AMBROSIA DELTOIDEA POLLEN (UNII: O4AB4546TP)
  • AMBROSIA DELTOIDEA POLLEN (UNII: O4AB4546TP) (Active Moiety)
  • CELTIS OCCIDENTALIS POLLEN (UNII: 68R9X9Y96X)
  • CELTIS OCCIDENTALIS POLLEN (UNII: 68R9X9Y96X) (Active Moiety)
  • AILANTHUS ALTISSIMA POLLEN (UNII: 2A64U81OQ3)
  • AILANTHUS ALTISSIMA POLLEN (UNII: 2A64U81OQ3) (Active Moiety)
  • AMBROSIA ACANTHICARPA POLLEN (UNII: U2AI3H2J5Y)
  • AMBROSIA ACANTHICARPA POLLEN (UNII: U2AI3H2J5Y) (Active Moiety)
  • SARCOBATUS VERMICULATUS POLLEN (UNII: 6532U64A3X)
  • SARCOBATUS VERMICULATUS POLLEN (UNII: 6532U64A3X) (Active Moiety)
  • AMBROSIA TRIFIDA POLLEN (UNII: KU1V1898XX)
  • AMBROSIA TRIFIDA POLLEN (UNII: KU1V1898XX) (Active Moiety)
  • SALSOLA KALI POLLEN (UNII: 2MH135KC6G)
  • SALSOLA KALI POLLEN (UNII: 2MH135KC6G) (Active Moiety)
  • ARTEMISIA TRIDENTATA POLLEN (UNII: YI19RB8YFD)
  • ARTEMISIA TRIDENTATA POLLEN (UNII: YI19RB8YFD) (Active Moiety)
  • ATRIPLEX WRIGHTII POLLEN (UNII: YB1308W43O)
  • ATRIPLEX WRIGHTII POLLEN (UNII: YB1308W43O) (Active Moiety)
  • RUMEX ACETOSELLA POLLEN (UNII: N52MIQ81ZW)
  • RUMEX ACETOSELLA POLLEN (UNII: N52MIQ81ZW) (Active Moiety)
  • AMBROSIA PSILOSTACHYA POLLEN (UNII: RX18M46K8L)
  • AMBROSIA PSILOSTACHYA POLLEN (UNII: RX18M46K8L) (Active Moiety)
  • ATRIPLEX CANESCENS POLLEN (UNII: 26U0BU8G83)
  • ATRIPLEX CANESCENS POLLEN (UNII: 26U0BU8G83) (Active Moiety)
  • ARTEMISIA ABSINTHIUM POLLEN (UNII: 81GS97HVFO)
  • ARTEMISIA ABSINTHIUM POLLEN (UNII: 81GS97HVFO) (Active Moiety)

Which are Wormwood Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

What is the NDC to RxNorm Crosswalk for Wormwood?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • RxCUI: 1006357 - Russian thistle pollen extract 20000 UNT/ML Injectable Solution
  • RxCUI: 1006357 - Salsola kali pollen extract 20,000 UNT/ML Injectable Solution
  • RxCUI: 1006365 - Canada goldenrod pollen extract 20,000 UNT/mL Injectable Solution
  • RxCUI: 1006365 - Canada goldenrod pollen extract 20000 UNT/ML Injectable Solution
  • RxCUI: 1006365 - Solidago canadensis pollen extract 20,000 UNT/ML Injectable Solution

* Please review the disclaimer below.

Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".