NDC 76144-611 Paulas Choice Clear Daily Skin Clearing Treatment
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 76144 - Paula's Choice, Llc
- 76144-611 - Paulas Choice Clear Daily Skin Clearing Treatment
Product Packages
NDC Code 76144-611-01
Package Description: 67 mL in 1 TUBE
NDC Code 76144-611-02
Package Description: 15 mL in 1 TUBE
NDC Code 76144-611-03
Package Description: 2 mL in 1 PACKET
Product Details
What is NDC 76144-611?
What are the uses for Paulas Choice Clear Daily Skin Clearing Treatment?
Which are Paulas Choice Clear Daily Skin Clearing Treatment UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZOYL PEROXIDE (UNII: W9WZN9A0GM)
- BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (Active Moiety)
Which are Paulas Choice Clear Daily Skin Clearing 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:
- LEVOMENOL (UNII: 24WE03BX2T)
- ALLANTOIN (UNII: 344S277G0Z)
- CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- WATER (UNII: 059QF0KO0R)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- HYDROXYETHYL CELLULOSE (5000 CPS AT 1%) (UNII: X70SE62ZAR)
- LAURETH-4 (UNII: 6HQ855798J)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
What is the NDC to RxNorm Crosswalk for Paulas Choice Clear Daily Skin Clearing Treatment?
- RxCUI: 106309 - benzoyl peroxide 5 % Topical Lotion
- RxCUI: 106309 - benzoyl peroxide 50 MG/ML Topical Lotion
* Please review the disclaimer below.
Patient Education
Benzoyl Peroxide Topical
Benzoyl peroxide is used to treat mild to moderate acne.
[Learn More]
Benzoyl Peroxide Topical
Benzoyl peroxide is used to treat mild to moderate acne.
[Learn More]
* 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".