NDC 66163-4454 Raf Five - After Hours Salicylic Acid Moisturizing
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 66163 - Cosmetic Solutions Llc
- 66163-4454 - Raf Five - After Hours Salicylic Acid Moisturizing
Product Packages
NDC Code 66163-4454-1
Package Description: 50 mL in 1 BOTTLE
Product Details
What is NDC 66163-4454?
What are the uses for Raf Five - After Hours Salicylic Acid Moisturizing?
Which are Raf Five - After Hours Salicylic Acid Moisturizing 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 Raf Five - After Hours Salicylic Acid Moisturizing 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)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- PPG-12/SMDI COPOLYMER (UNII: 1BK9DDD24E)
- NIACINAMIDE (UNII: 25X51I8RD4)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- SQUALANE (UNII: GW89575KF9)
- CETEARYL OLIVATE (UNII: 58B69Q84JO)
- HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%) (UNII: 86FQE96TZ4)
- GLYCERYL MONOCAPRYLATE (UNII: TM2TZD4G4A)
- SORBITAN OLIVATE (UNII: MDL271E3GR)
- CANNABIDIOL (UNII: 19GBJ60SN5)
- ERGOTHIONEINE (UNII: BDZ3DQM98W)
- GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- ARTEMISIA VULGARIS TOP OIL (UNII: 72Q967Y48V)
- BERGAMOT OIL (UNII: 39W1PKE3JI)
- LEMON OIL, COLD PRESSED (UNII: I9GRO824LL)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- JUNIPERUS VIRGINIANA OIL (UNII: PAD4FN7P2G)
- SPEARMINT OIL (UNII: C3M81465G5)
- GRAPE SEED OIL (UNII: 930MLC8XGG)
- GLYCERIN (UNII: PDC6A3C0OX)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- POLYDEXTROSE (UNII: VH2XOU12IE)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
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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".