NDC 37945-894 Kleer-plex Targeted Acne Pen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 37945 - Bio-medical & Pharmaceutical Manufacturing Corporation
- 37945-894 - Kleer-plex Targeted Acne Pen
Product Details
What is NDC 37945-894?
What are the uses for Kleer-plex Targeted Acne Pen?
Which are Kleer-plex Targeted Acne Pen 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 Kleer-plex Targeted Acne Pen 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:
- BRUCINE SULFATE (UNII: KY7O12XPOQ)
- WATER (UNII: 059QF0KO0R)
- ALCOHOL (UNII: 3K9958V90M)
- GLYCERIN (UNII: PDC6A3C0OX)
- XANTHAN GUM (UNII: TTV12P4NEE)
- PEPPERMINT (UNII: V95R5KMY2B)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- WHEAT GERM OIL (UNII: 14C97E680P)
- GLYCOLIC ACID (UNII: 0WT12SX38S)
- TERT-BUTYL ALCOHOL (UNII: MD83SFE959)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
What is the NDC to RxNorm Crosswalk for Kleer-plex Targeted Acne Pen?
- RxCUI: 1591999 - Kleer Plex 2 % Topical Gel
- RxCUI: 1591999 - salicylic acid 0.02 MG/MG Topical Gel [Kleer Plex]
- RxCUI: 1591999 - Kleer Plex 0.02 MG/MG Topical Gel
- RxCUI: 346298 - salicylic acid 2 % Topical Gel
- RxCUI: 346298 - salicylic acid 0.02 MG/MG Topical Gel
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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".