NDC 14222-1600 Spotless Regimen For Acne, Blemishes And Breakouts
Benzoyl Peroxide Kit Topical - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 14222 - Rodan & Fields
- 14222-1600 - Spotless Regimen For Acne, Blemishes And Breakouts
Product Packages
NDC Code 14222-1600-1
Package Description: 1 KIT in 1 CARTON * 1 TUBE in 1 CARTON (14222-1610-1) / 125 mL in 1 TUBE * 1 BOTTLE, PUMP in 1 CARTON (14222-1620-1) / 50 mL in 1 BOTTLE, PUMP
Product Details
What is NDC 14222-1600?
What are the uses for Spotless Regimen For Acne, Blemishes And Breakouts?
Which are Spotless Regimen For Acne, Blemishes And Breakouts 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 Spotless Regimen For Acne, Blemishes And Breakouts 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)
- POLYACRYLAMIDE (10000 MW) (UNII: E2KR9C9V2I)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- DOCUSATE SODIUM (UNII: F05Q2T2JA0)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- HYDROGENATED JOJOBA OIL, RANDOMIZED (UNII: Q47ST02F58)
- LAURETH-7 (UNII: Z95S6G8201)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- PROPANEDIOL (UNII: 5965N8W85T)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- GLYCERETH-18 ETHYLHEXANOATE (UNII: IWS58C6V2Y)
- GLYCERETH-18 (UNII: SA5E43C17C)
- GLYCERIN (UNII: PDC6A3C0OX)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- ALLANTOIN (UNII: 344S277G0Z)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CETYL HYDROXYETHYLCELLULOSE (350000 MW) (UNII: T7SWE4S2TT)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- D&C RED NO. 33 (UNII: 9DBA0SBB0L)
- D&C VIOLET NO. 2 (UNII: 350KA7O6HK)
- DECYLENE GLYCOL (UNII: S57M60MI88)
- DIMETHYL ISOSORBIDE (UNII: SA6A6V432S)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- GINGER (UNII: C5529G5JPQ)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
- HYDROXYPHENYL PROPAMIDOBENZOIC ACID (UNII: 25KRT26H77)
- ISOHEXADECANE (UNII: 918X1OUF1E)
- LEVOMENOL (UNII: 24WE03BX2T)
- LOWBUSH BLUEBERRY (UNII: G90PX41VP0)
- METHYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER (UNII: 657L0NC5MT)
- MICA (UNII: V8A1AW0880)
- MYRISTYL ALCOHOL (UNII: V42034O9PU)
- OCTENIDINE HYDROCHLORIDE (UNII: U84956NU4B)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- PHYTOSTERYL/OCTYLDODECYL LAUROYL GLUTAMATE (UNII: 65954KGO9Q)
- PIDOLIC ACID (UNII: SZB83O1W42)
- POLYGLYCERYL-2 MONOISOSTEARATE (UNII: 7B8OE71MQC)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- REYNOUTRIA JAPONICA ROOT (UNII: 7TRV45YZF7)
- SODIUM ACRYLOYLDIMETHYLTAURATE-ACRYLAMIDE COPOLYMER (1:1; 90000-150000 MPA.S) (UNII: 5F4963KLHS)
- SORBITAN MONOOLEATE (UNII: 06XEA2VD56)
- STANNIC OXIDE (UNII: KM7N50LOS6)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TOCOPHEROL (UNII: R0ZB2556P8)
- XANTHAN GUM (UNII: TTV12P4NEE)
What is the NDC to RxNorm Crosswalk for Spotless Regimen For Acne, Blemishes And Breakouts?
- RxCUI: 200009 - benzoyl peroxide 2.5 % Topical Lotion
- RxCUI: 200009 - benzoyl peroxide 25 MG/ML Topical Lotion
- RxCUI: 308696 - benzoyl peroxide 5 % Medicated Liquid Soap
- RxCUI: 308696 - benzoyl peroxide 50 MG/ML Medicated Liquid Soap
* Please review the disclaimer below.
[1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
[3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
[4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[6] What is the FDA Application Number? - This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
[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".