NDC 70367-004 Pumice Cleansing Scrub- 2.5% Benzoyl Peroxide
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 70367 - Only Yourx, Inc.
- 70367-004 - Pumice Cleansing Scrub- 2.5% Benzoyl Peroxide
Product Characteristics
Product Packages
NDC Code 70367-004-04
Package Description: 120 mL in 1 TUBE
NDC Code 70367-004-08
Package Description: 240 mL in 1 TUBE
NDC Code 70367-004-75
Package Description: 22.18 mL in 1 TUBE
Product Details
What is NDC 70367-004?
What are the uses for Pumice Cleansing Scrub- 2.5% Benzoyl Peroxide?
Which are Pumice Cleansing Scrub- 2.5% Benzoyl Peroxide 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 Pumice Cleansing Scrub- 2.5% Benzoyl Peroxide 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:
- SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ETHOXYDIGLYCOL BEHENATE (UNII: N76ISC4ZZO)
- GLYCERIN (UNII: PDC6A3C0OX)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
What is the NDC to RxNorm Crosswalk for Pumice Cleansing Scrub- 2.5% Benzoyl Peroxide?
- RxCUI: 845836 - benzoyl peroxide 2.5 % Medicated Liquid Soap
- RxCUI: 845836 - benzoyl peroxide 25 MG/ML Medicated Liquid Soap
* Please review the disclaimer below.
Patient Education
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".