NDC 52664-007 Elf Zit Zapper
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 52664-007?
What are the uses for Elf Zit Zapper?
Which are Elf Zit Zapper UNII Codes?
The UNII codes for the active ingredients in this product are:
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Elf Zit Zapper 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)
- HAMAMELIS VIRGINIANA LEAF (UNII: T07U1161SV)
- ALCOHOL (UNII: 3K9958V90M)
- TEA TREE OIL (UNII: VIF565UC2G)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- LAURETH-7 (UNII: Z95S6G8201)
- CAMPHOR OIL (UNII: 75IZZ8Y727)
What is the NDC to RxNorm Crosswalk for Elf Zit Zapper?
- RxCUI: 1047362 - salicylic acid 1 % Topical Solution
- RxCUI: 1047362 - salicylic acid 10 MG/ML Topical 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".