NDC 36987-1127 House Dust
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 36987 - Nelco Laboratories, Inc.
- 36987-1127 - House Dust
Product Packages
NDC Code 36987-1127-1
Package Description: 5 mL in 1 VIAL, MULTI-DOSE
NDC Code 36987-1127-2
Package Description: 10 mL in 1 VIAL, MULTI-DOSE
NDC Code 36987-1127-3
Package Description: 30 mL in 1 VIAL, MULTI-DOSE
NDC Code 36987-1127-4
Package Description: 50 mL in 1 VIAL, MULTI-DOSE
Product Details
What is NDC 36987-1127?
What are the uses for House Dust?
Which are House 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 House 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:
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM BICARBONATE (UNII: 8MDF5V39QO)
- WATER (UNII: 059QF0KO0R)
- PHENOL (UNII: 339NCG44TV)
- GLYCERIN (UNII: PDC6A3C0OX)
What is the NDC to RxNorm Crosswalk for House Dust?
- RxCUI: 307922 - house dust allergenic extract 10,000 UNT/mL Injectable Solution
- RxCUI: 307922 - house dust allergenic extract 10000 UNT/ML Injectable Solution
- RxCUI: 307922 - house dust extract 10,000 UNT/ML Injectable Solution
- RxCUI: 307923 - house dust allergenic extract 20,000 UNT/mL Injectable Solution
- RxCUI: 307923 - house dust allergenic extract 20000 UNT/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".