NDC 42254-065 Lice Treatment
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 42254 - Rebel Distributors Corp
- 42254-065 - Lice Treatment
Product Packages
NDC Code 42254-065-60
Package Description: 1 BOTTLE in 1 CARTON / 59 mL in 1 BOTTLE
Product Details
What is NDC 42254-065?
What are the uses for Lice Treatment?
Which are Lice Treatment UNII Codes?
The UNII codes for the active ingredients in this product are:
- PERMETHRIN (UNII: 509F88P9SZ)
- PERMETHRIN (UNII: 509F88P9SZ) (Active Moiety)
Which are Lice Treatment 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:
- CANADA BALSAM (UNII: K304VI98I3)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- CETETH-10 (UNII: LF9X1PN3XJ)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- WATER (UNII: 059QF0KO0R)
- STEARALKONIUM CHLORIDE (UNII: 0OUO26BB88)
What is the NDC to RxNorm Crosswalk for Lice Treatment?
- RxCUI: 250387 - permethrin 1 % Medicated Shampoo
- RxCUI: 250387 - permethrin 10 MG/ML Medicated Shampoo
- RxCUI: 250387 - permethrin 1 % Topical Lotion
* Please review the disclaimer below.
[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".