NDC 80861-007 Acne Free Sensitive Skin 24 Hr Acne Clearing System
Salicylic Acid,Benzoyl Peroxide Kit - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 80861 - Acnefree Llc
- 80861-007 - Acne Free Sensitive Skin 24 Hr Acne Clearing System
Product Packages
NDC Code 80861-007-01
Package Description: 1 KIT in 1 KIT * 118 mL in 1 BOTTLE (80861-008-01) * 59 mL in 1 BOTTLE (80861-009-01)
Product Details
What is NDC 80861-007?
What are the uses for Acne Free Sensitive Skin 24 Hr Acne Clearing System?
Which are Acne Free Sensitive Skin 24 Hr Acne Clearing System 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 Acne Free Sensitive Skin 24 Hr Acne Clearing System 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 COCOYL ISETHIONATE (UNII: 518XTE8493)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- SODIUM LAUROAMPHOACETATE (UNII: SLK428451L)
- DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E)
- GLYCOL DISTEARATE (UNII: 13W7MDN21W)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- OAT (UNII: Z6J799EAJK)
- PHYTATE SODIUM (UNII: 88496G1ERL)
- ZINC PIDOLATE (UNII: C32PQ86DH4)
- GLYCERIN (UNII: PDC6A3C0OX)
- SORBIC ACID (UNII: X045WJ989B)
- ETHYL VANILLIN (UNII: YC9ST449YJ)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- PSEUDOPTEROGORGIA ELISABETHAE (UNII: UDY3H1OUX5)
- AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
- ETHYL MACADAMIATE (UNII: ANA2NCS6V1)
- PROPANEDIOL (UNII: 5965N8W85T)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- LEVOMENOL (UNII: 24WE03BX2T)
- LAURETH-7 (UNII: Z95S6G8201)
- ALLANTOIN (UNII: 344S277G0Z)
- TEA TREE OIL (UNII: VIF565UC2G)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- METHYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER (UNII: EG97988M5Q)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- GINGER (UNII: C5529G5JPQ)
What is the NDC to RxNorm Crosswalk for Acne Free Sensitive Skin 24 Hr Acne Clearing System?
- RxCUI: 1234456 - salicylic acid 1.5 % Medicated Liquid Soap
- RxCUI: 1234456 - salicylic acid 15 MG/ML Medicated Liquid Soap
- RxCUI: 1548871 - benzoyl peroxide 3 % Topical Lotion
- RxCUI: 1548871 - benzoyl peroxide 30 MG/ML Topical Lotion
- RxCUI: 1549098 - {1 (59 ML) (benzoyl peroxide 30 MG/ML Topical Lotion) / 1 (118 ML) (salicylic acid 15 MG/ML Medicated Liquid Soap) } Pack
* Please review the disclaimer below.
Patient Education
Benzoyl Peroxide Topical
Benzoyl peroxide is used to treat mild to moderate acne.
[Learn More]
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.
[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".