NDC 63940-536 Oil-free Acne Wash
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63940 - Harmon Stores Inc
- 63940-536 - Oil-free Acne Wash
Product Packages
NDC Code 63940-536-11
Package Description: 269 mL in 1 BOTTLE
Product Details
What is NDC 63940-536?
What are the uses for Oil-free Acne Wash?
Which are Oil-free Acne Wash 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 Oil-free Acne Wash 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:
- SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)
- WATER (UNII: 059QF0KO0R)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SORBITAN MONOLAURATE (UNII: 6W9PS8B71J)
- C12-15 ALKYL LACTATE (UNII: GC844VRD7E)
- COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- CHAMOMILE (UNII: FGL3685T2X)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
What is the NDC to RxNorm Crosswalk for Oil-free Acne Wash?
- 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".