NDC 76413-350 Sunmark Lice Killing Maximum Strength Lice Treatment
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 76413 - Central Texas Community Health Centers
- 76413-350 - Sunmark Lice Killing
Product Characteristics
Product Packages
NDC Code 76413-350-01
Package Description: 1 BOTTLE in 1 CARTON / 118 mL in 1 BOTTLE
Product Details
What is NDC 76413-350?
What are the uses for Sunmark Lice Killing Maximum Strength Lice Treatment?
Which are Sunmark Lice Killing Maximum Strength Lice Treatment UNII Codes?
The UNII codes for the active ingredients in this product are:
- PIPERONYL BUTOXIDE (UNII: LWK91TU9AH)
- PIPERONYL BUTOXIDE (UNII: LWK91TU9AH) (Active Moiety)
- PYRETHRUM EXTRACT (UNII: ZUM06L90GV)
- PYRETHRUM EXTRACT (UNII: ZUM06L90GV) (Active Moiety)
Which are Sunmark Lice Killing Maximum Strength 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:
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- WATER (UNII: 059QF0KO0R)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- XANTHAN GUM (UNII: TTV12P4NEE)
What is the NDC to RxNorm Crosswalk for Sunmark Lice Killing Maximum Strength Lice Treatment?
- RxCUI: 283219 - piperonyl butoxide 4 % / pyrethrins 0.33 % Medicated Shampoo
- RxCUI: 283219 - piperonyl butoxide 40 MG/ML / pyrethrins 3.3 MG/ML 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".