NDC 69842-082 Skinpharmacy Advanced Acne Therapy Kit
Salicylic Acid,Benzoyl Peroxide Kit Topical - View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 69842-082?
What are the uses for Skinpharmacy Advanced Acne Therapy Kit?
Which are Skinpharmacy Advanced Acne Therapy Kit UNII Codes?
The UNII codes for the active ingredients in this product are:
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
- BENZOYL PEROXIDE (UNII: W9WZN9A0GM)
- BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (Active Moiety)
Which are Skinpharmacy Advanced Acne Therapy Kit 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)
- POLYETHYLENE GLYCOL 4000 (UNII: 4R4HFI6D95)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- XANTHAN GUM (UNII: TTV12P4NEE)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
- HAMAMELIS VIRGINIANA FLOWER WATER (UNII: 222MYC9QUV)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
- LICORICE (UNII: 61ZBX54883)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- LAURYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER (UNII: EX0F4CZ66H)
- GLYCERIN (UNII: PDC6A3C0OX)
- METHYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER (UNII: EG97988M5Q)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- SORBITOL (UNII: 506T60A25R)
- GLYCERYL DILAURATE (UNII: MFL3ZIE8SK)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
What is the NDC to RxNorm Crosswalk for Skinpharmacy Advanced Acne Therapy Kit?
- RxCUI: 106309 - benzoyl peroxide 5 % Topical Lotion
- RxCUI: 106309 - benzoyl peroxide 50 MG/ML Topical Lotion
- RxCUI: 1874139 - {1 (22 ML) (benzoyl peroxide 25 MG/ML Topical Lotion) / 1 (12 ML) (benzoyl peroxide 50 MG/ML Topical Lotion) / 1 (118 ML) (salicylic acid 20 MG/ML Medicated Liquid Soap) } Pack
- RxCUI: 1874139 - benzyol peroxide 2.5 % Topical Lotion (22 ML) / benzyol peroxide 5 % Topical Lotion (12 ML) / salicylic acid 2 % Medicated Liqiud Soap (118 ML) Pack
- RxCUI: 200009 - benzoyl peroxide 2.5 % Topical Lotion
* Please review the disclaimer below.
Patient Education
Benzoyl Peroxide Topical
Benzoyl peroxide is used to treat mild to moderate acne.
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Salicylic Acid Topical
Topical salicylic acid is used to help clear and prevent pimples and skin blemishes in people who have acne. Topical salicylic acid is also used to treat skin conditions that involve scaling or overgrowth of skin cells such as psoriasis (a skin disease in which red, scaly patches form on some areas of the body), ichthyoses (inborn conditions that cause skin dryness and scaling), dandruff, corns, calluses, and warts on the hands or feet. Topical salicylic acid should not be used to treat genital warts, warts on the face, warts with hair growing from them, warts in the nose or mouth, moles, or birthmarks. Salicylic acid is in a class of medications called keratolytic agents. Topical salicylic acid treats acne by reducing swelling and redness and unplugging blocked skin pores to allow pimples to shrink. It treats other skin conditions by softening and loosening dry, scaly, or thickened skin so that it falls off or can be removed easily.
[Learn More]
* 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".