NDC 0363-7784 Spot Acne Treatment
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 0363 - Walgreens
- 0363-7784 - Spot Acne Treatment
Product Packages
NDC Code 0363-7784-01
Package Description: 1 TUBE in 1 CARTON / 21 g in 1 TUBE
Product Details
What is NDC 0363-7784?
Which are Spot Acne 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 Spot Acne 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:
- BENTONITE (UNII: A3N5ZCN45C)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERYL LAURATE (UNII: Y98611C087)
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- WATER (UNII: 059QF0KO0R)
- XANTHAN GUM (UNII: TTV12P4NEE)
What is the NDC to RxNorm Crosswalk for Spot Acne Treatment?
- RxCUI: 200009 - benzoyl peroxide 2.5 % Topical Lotion
- RxCUI: 200009 - benzoyl peroxide 25 MG/ML Topical Lotion
* 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".