NDC 36987-1816 Mosquito
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Product Details
What is NDC 36987-1816?
What are the uses for Mosquito?
Which are Mosquito 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)
- ALLERGENIC EXTRACT- COCKROACH PERIPLANETA AMERICANA (UNII: 2RQ1L9N089)
- ALLERGENIC EXTRACT- COCKROACH PERIPLANETA AMERICANA (UNII: 2RQ1L9N089) (Active Moiety)
- AEDES TAENIORHYNCHUS (UNII: BN2DNW66IQ)
- AEDES TAENIORHYNCHUS (UNII: BN2DNW66IQ) (Active Moiety)
Which are Mosquito 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 Mosquito?
- RxCUI: 905099 - mosquito allergenic extract 50 MG/ML Injectable Solution
- RxCUI: 905099 - Aedes taeniorhynchus allergenic extract 50 MG/ML Injectable Solution
- RxCUI: 905099 - mosquito allergenic extract 0.05 GM/ML Injectable Solution
- RxCUI: 905261 - American cockroach allergenic extract 50 MG/ML Injectable Solution
- RxCUI: 905261 - American cockroach allergenic extract 0.05 GM/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".