NDC 49288-0181 A. Dust
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Packages
NDC Code 49288-0181-1
Package Description: 2 mL in 1 VIAL, MULTI-DOSE
NDC Code 49288-0181-2
Package Description: 5 mL in 1 VIAL, MULTI-DOSE
NDC Code 49288-0181-3
Package Description: 10 mL in 1 VIAL, MULTI-DOSE
NDC Code 49288-0181-4
Package Description: 30 mL in 1 VIAL, MULTI-DOSE
NDC Code 49288-0181-5
Package Description: 50 mL in 1 VIAL, MULTI-DOSE
Product Details
What is NDC 49288-0181?
What are the uses for A. Dust?
Which are A. Dust UNII Codes?
The UNII codes for the active ingredients in this product are:
- HOUSE DUST (UNII: EYO007VX98)
- HOUSE DUST (UNII: EYO007VX98) (Active Moiety)
Which are A. Dust 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:
- GLYCERIN (UNII: PDC6A3C0OX)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM BICARBONATE (UNII: 8MDF5V39QO)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for A. Dust?
- RxCUI: 901358 - house dust allergenic extract 50 MG/mL Injectable Solution
- RxCUI: 901358 - house dust allergenic extract 50 MG/ML Injectable Solution
- RxCUI: 901358 - house dust allergenic extract 0.05 GM/ML Injectable Solution
- RxCUI: 901358 - house dust allergenic extract 1 GM per 20 ML Injectable Solution
- RxCUI: 901358 - house dust extract 50 MG/ML Injectable Solution
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[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".