NDC 62742-4070 Clarifying Toner
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 62742 - Allure Labs, Inc
- 62742-4070 - Clarifying Toner
Product Packages
NDC Code 62742-4070-1
Package Description: 120 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 62742-4070?
What are the uses for Clarifying Toner?
Which are Clarifying Toner 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 Clarifying Toner 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 TOP WATER (UNII: NT00Y05A2V)
- GLYCERIN (UNII: PDC6A3C0OX)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- COMFREY ROOT (UNII: M9VVZ08EKQ)
- PLANTAGO OVATA SEED (UNII: UD50RBY30F)
- SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
- HYDROLYZED WHEAT PROTEIN (ENZYMATIC, 3000 MW) (UNII: J2S07SB0YL)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- ROSEMARY (UNII: IJ67X351P9)
- CHAMOMILE (UNII: FGL3685T2X)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- ALLANTOIN (UNII: 344S277G0Z)
- GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
What is the NDC to RxNorm Crosswalk for Clarifying Toner?
- 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".