NDC 63868-777 Acne Cleanser Awaken By Quality Choice
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63868 - Quality Choice
- 63868-777 - Acne Cleanser
Product Packages
NDC Code 63868-777-05
Package Description: 177 mL in 1 BOTTLE
Product Details
What is NDC 63868-777?
What are the uses for Acne Cleanser Awaken By Quality Choice?
Which are Acne Cleanser Awaken By Quality Choice 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 Acne Cleanser Awaken By Quality Choice 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 C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- CHAMOMILE (UNII: FGL3685T2X)
- COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- ALOE (UNII: V5VD430YW9)
- CHAMAEMELUM NOBILE FLOWER (UNII: O2T154T6OG)
- C12-15 ALKYL LACTATE (UNII: GC844VRD7E)
- PEG-80 SORBITAN LAURATE (UNII: 239B50Y732)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
What is the NDC to RxNorm Crosswalk for Acne Cleanser Awaken By Quality Choice?
- 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
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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".