NDC 36987-1786 House Fly
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 36987 - Nelco Laboratories, Inc.
- 36987-1786 - House Fly
Product Packages
NDC Code 36987-1786-1
Package Description: 5 mL in 1 VIAL, MULTI-DOSE
NDC Code 36987-1786-2
Package Description: 10 mL in 1 VIAL, MULTI-DOSE
NDC Code 36987-1786-3
Package Description: 30 mL in 1 VIAL, MULTI-DOSE
NDC Code 36987-1786-4
Package Description: 50 mL in 1 VIAL, MULTI-DOSE
Product Details
What is NDC 36987-1786?
What are the uses for House Fly?
Which are House Fly UNII Codes?
The UNII codes for the active ingredients in this product are:
- SOLENOPSIS INVICTA (UNII: 5O7CR4P444)
- SOLENOPSIS INVICTA (UNII: 5O7CR4P444) (Active Moiety)
- MUSCA DOMESTICA (UNII: PV7823W303)
- MUSCA DOMESTICA (UNII: PV7823W303) (Active Moiety)
Which are House Fly 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)
- PHENOL (UNII: 339NCG44TV)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for House Fly?
- RxCUI: 905111 - mosquito allergenic extract 10000 UNT/ML Injectable Solution
- RxCUI: 905111 - Aedes taeniorhynchus allergenic extract 10,000 UNT/ML Injectable Solution
- RxCUI: 905264 - American cockroach allergenic extract 10000 UNT/ML Injectable Solution
- RxCUI: 905264 - Blatta americana allergenic extract 10,000 UNT/ML Injectable Solution
- RxCUI: 905264 - Periplaneta americana allergenic extract 10,000 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".