NDC 0363-0910 Charcoal Blackhead Clearing Scrub
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 0363 - Walgreen Co
- 0363-0910 - Charcoal Blackhead Clearing Scrub
Product Packages
NDC Code 0363-0910-28
Package Description: 148 mL in 1 TUBE
Product Details
What is NDC 0363-0910?
What are the uses for Charcoal Blackhead Clearing Scrub?
Which are Charcoal Blackhead Clearing Scrub UNII Codes?
The UNII codes for the active ingredients in this product are:
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Charcoal Blackhead Clearing Scrub 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)
- SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
- SYNTHETIC WAX (1200 MW) (UNII: Q3Z4BCH099)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L)
- COCO-BETAINE (UNII: 03DH2IZ3FY)
- COCO MONOETHANOLAMIDE (UNII: C80684146D)
- GLYCERIN (UNII: PDC6A3C0OX)
- ACTIVATED CHARCOAL (UNII: 2P3VWU3H10)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- POLYGLYCERIN-10 (UNII: P9060O936A)
- POLYGLYCERYL-10 STEARATE (UNII: 90TF85HH91)
- PPG-5-CETETH-20 (UNII: 4AAN25P8P4)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
What is the NDC to RxNorm Crosswalk for Charcoal Blackhead Clearing Scrub?
- RxCUI: 562600 - salicylic acid 2 % Medicated Liquid Soap
- RxCUI: 562600 - salicylic acid 20 MG/ML Medicated Liquid Soap
- RxCUI: 562600 - salicylic acid 2 % Facial Cleanser Toner
- RxCUI: 562600 - salicylic acid 2 % Facial Scrub
* 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".