NDC 0363-7783 Tinted Acne Treatment
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 0363 - Walgreens
- 0363-7783 - Tinted Acne Treatment
Product Packages
NDC Code 0363-7783-01
Package Description: 1 TUBE in 1 CARTON / 18 g in 1 TUBE
Product Details
What is NDC 0363-7783?
Which are Tinted Acne Treatment UNII Codes?
The UNII codes for the active ingredients in this product are:
- RESORCINOL (UNII: YUL4LO94HK)
- RESORCINOL (UNII: YUL4LO94HK) (Active Moiety)
- SULFUR (UNII: 70FD1KFU70)
- SULFUR (UNII: 70FD1KFU70) (Active Moiety)
Which are Tinted 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:
- WATER (UNII: 059QF0KO0R)
- ALCOHOL (UNII: 3K9958V90M)
- BENTONITE (UNII: A3N5ZCN45C)
- GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERROUS OXIDE (UNII: G7036X8B5H)
What is the NDC to RxNorm Crosswalk for Tinted Acne Treatment?
- RxCUI: 312793 - resorcinol 2 % / sulfur 8 % Topical Cream
- RxCUI: 312793 - resorcinol 20 MG/ML / sulfur 80 MG/ML Topical Cream
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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".