NDC 49825-129 Breakout Control Bioelements
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 49825 - Bioelements, Inc.
- 49825-129 - Breakout Control
Product Packages
NDC Code 49825-129-02
Package Description: 1 BOTTLE in 1 CARTON / 29 mL in 1 BOTTLE (49825-129-01)
Product Details
What is NDC 49825-129?
What are the uses for Breakout Control Bioelements?
Which are Breakout Control Bioelements 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 Breakout Control Bioelements 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)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4)
- SQUALANE (UNII: GW89575KF9)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- FYTIC ACID (UNII: 7IGF0S7R8I)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
What is the NDC to RxNorm Crosswalk for Breakout Control Bioelements?
- RxCUI: 308693 - benzoyl peroxide 5 % Topical Cream
- RxCUI: 308693 - benzoyl peroxide 50 MG/ML Topical Cream
* 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".