NDC 14222-2000 Unblemish
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 14222 - Rodan & Fields, Llc
- 14222-2000 - Unblemish
Product Packages
NDC Code 14222-2000-2
Package Description: 1 BOTTLE, PUMP in 1 CARTON / 22.5 mL in 1 BOTTLE, PUMP
Product Details
What is NDC 14222-2000?
What are the uses for Unblemish?
Which are Unblemish UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZOYL PEROXIDE (UNII: W9WZN9A0GM)
- BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (Active Moiety)
Which are Unblemish 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:
- ALLANTOIN (UNII: 344S277G0Z)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- BIOSACCHARIDE GUM-1 (UNII: BB4PU4V09H)
- CARBOMER 934 (UNII: Z135WT9208)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- CERAMIDE 6 II (UNII: F1X8L2B00J)
- CERAMIDE 1 (UNII: 5THT33P7X7)
- CERAMIDE 3 (UNII: 4370DF050B)
- CHAMOMILE (UNII: FGL3685T2X)
- CHOLESTEROL (UNII: 97C5T2UQ7J)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- DISODIUM OLEAMIDO MEA-SULFOSUCCINATE (UNII: 5M1101WGSY)
- GLYCERIN (UNII: PDC6A3C0OX)
- LAURETH-7 (UNII: Z95S6G8201)
- NIACINAMIDE (UNII: 25X51I8RD4)
- PANTHENOL (UNII: WV9CM0O67Z)
- PHYTOSPHINGOSINE (UNII: GIN46U9Q2Q)
- SODIUM ACRYLOYLDIMETHYLTAURATE-ACRYLAMIDE COPOLYMER (1:1; 90000-150000 MPA.S) (UNII: 5F4963KLHS)
- PUNICA GRANATUM ROOT BARK (UNII: CLV24I3T1D)
- WATER (UNII: 059QF0KO0R)
- SODIUM LAUROYL LACTYLATE (UNII: 7243K85WFO)
- XANTHAN GUM (UNII: TTV12P4NEE)
- YUCCA GLAUCA ROOT (UNII: 1A15YBH7N1)
What is the NDC to RxNorm Crosswalk for Unblemish?
- RxCUI: 106309 - benzoyl peroxide 5 % Topical Lotion
- RxCUI: 106309 - benzoyl peroxide 50 MG/ML Topical Lotion
* 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".