NDC 65044-2052 Pollens - Trees, Olive Olea Europaea

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:
65044-2052
Proprietary Name:
Pollens - Trees, Olive Olea Europaea
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Jubilant Hollisterstier Llc
Labeler Code:
65044
Start Marketing Date: [9]
04-19-1941
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 65044-2052-5

Package Description: 5 mL in 1 VIAL

Product Details

What is NDC 65044-2052?

The NDC code 65044-2052 is assigned by the FDA to the product Pollens - Trees, Olive Olea Europaea which is product labeled by Jubilant Hollisterstier Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 65044-2052-5 5 ml in 1 vial . 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 Pollens - Trees, Olive Olea Europaea?

Certain diagnostics carry labeling which states Allergenic Extract for Diagnostic Use Only. Data to support the therapeutic use of products labeled with this statement have not been established.15In addition to a carefully taken history, the use of intradermal testing extracts is an accepted method in the diagnosis of allergenic conditions.1, 2, 3 When scratch, prick or puncture reactions are small, or if the patient gives a history of allergic symptoms to a substance but scratch, prick or puncture tests are inconclusive, intradermal tests may be indicated. However, ANTIGENS PRODUCING LARGE 3 TO 4+ SCRATCH, PRICK OR PUNCTURE TESTS SHOULD NOT BE TESTED INTRADERMALLY. Extracts of all allergens do not produce equivalent results in intradermal testing. The intensity of the skin reaction produced will be determined by two factors: the degree of sensitivity of the patient and the nature of the antigenic extract applied. In general, pollen extracts produce whealing reactions, whereas other inhalants produce erythematous reactions with wheals less often. Skin tests to foods seldom produce whealing reactions except for infrequent instances of severe sensitivity to fish, nuts or spices, and rarely other foods.

Which are Pollens - Trees, Olive Olea Europaea UNII Codes?

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

Which are Pollens - Trees, Olive Olea Europaea 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 Pollens - Trees, Olive Olea Europaea?

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: 1006369 - Canada goldenrod pollen extract 500 UNT/ML Injectable Solution
  • RxCUI: 1006369 - Solidago canadensis pollen extract 500 UNT/ML Injectable Solution
  • RxCUI: 1087970 - Mucor racemosus allergenic extract 1000 UNT/mL Injectable Solution
  • RxCUI: 1087970 - Mucor racemosus allergenic extract 1000 UNT/ML Injectable Solution
  • RxCUI: 1087970 - Mucor racemosus extract 1000 UNT/ML Injectable Solution

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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".