NDC 63736-210 Pronto Plus Lice Killing
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 63736-210?
What are the uses for Pronto Plus Lice Killing?
Which are Pronto Plus Lice Killing UNII Codes?
The UNII codes for the active ingredients in this product are:
- PYRETHRUM EXTRACT (UNII: ZUM06L90GV)
- PYRETHRUM EXTRACT (UNII: ZUM06L90GV) (Active Moiety)
- PIPERONYL BUTOXIDE (UNII: LWK91TU9AH)
- PIPERONYL BUTOXIDE (UNII: LWK91TU9AH) (Active Moiety)
Which are Pronto Plus Lice Killing 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:
- WATER (UNII: 059QF0KO0R)
- CANANGA OIL (UNII: 8YOY78GNNX)
- CHAMOMILE (UNII: FGL3685T2X)
- TEA TREE OIL (UNII: VIF565UC2G)
- PIMPINELLA ANISUM (UNII: HO63CL229O)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
What is the NDC to RxNorm Crosswalk for Pronto Plus Lice Killing?
- RxCUI: 283219 - piperonyl butoxide 4 % / pyrethrins 0.33 % Medicated Shampoo
- RxCUI: 283219 - piperonyl butoxide 40 MG/ML / pyrethrins 3.3 MG/ML Medicated Shampoo
- RxCUI: 729773 - Pronto Plus 4 % / 0.33 % Medicated Shampoo
- RxCUI: 729773 - piperonyl butoxide 40 MG/ML / pyrethrins 3.3 MG/ML Medicated Shampoo [Pronto Plus]
- RxCUI: 729773 - Pronto Maximum Strength (piperonyl butoxide 4 % / pyrethrins 0.33 % ) Medicated Shampoo
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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".