Label: ATRIX SYSTEM 1- salicylic acid kit
- NDC Code(s): 59088-445-08, 59088-446-05, 59088-713-00
- Packager: PureTek Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated December 13, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Atrix™ Acne Treatment Cream (2 fl oz ) 59 mL
- Drug Facts
- Active ingredient
- Purpose
- Uses:
- Warnings
-
Directions
■ Clean the skin thoroughly before applying this product
■ cover the entire affected area with a thin layer one to three times daily
■ because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor
■ if bothersome dryness or peeling occurs, reduce application to once a day or every other day.
Use under the direction of a medical practitioner.
- Other information
-
Inactive ingredients
Allyl Methacrylates Crosspolymer, Aqua (Purified Water), Butylene Glycol, Caprylyl Glycol, Carbomer, Cetearyl Olivate, Cyclopentasiloxane, Decyl Glucoside, Dimethicone, Dipotassium Glycyrrhizinate, Disodium EDTA, Ethylhexylglycerin, Alpha-Glucan Oligosaccharide, Glucosamine HCl, Glycerin, Glyceryl Stearate SE, Hexylene Glycol, Laminaria Digitata (Algae) Extract, Oligopeptide- 10, Palmitic Acid, Phenoxyethanol, Polysilicone-11, Saccharomyces Cerevisiae Extract, Sodium Ascorbyl Phosphate, Sodium Hydroxide, Sorbitan Olivate, Stearic Acid, DL- alpha- Tocopheryl Acetate, Urea
- QUESTIONS
- Atrix™ Antibacterial Wash (4 fl oz ) 118 mL
- Active ingredient
- Purpose
- Use
- Warnings
- Directions
- Other information
-
Inactive ingredients
Aqua (Purified Water), Cetyl Hydroxyethylcellulose, Citrus Paradisi (Grapefruit) Peel Oil, Cocamidopropyl Betaine, Disodium EDTA, Ethoxydiglycol, Glycerin, Lauryl Glucoside, Menthol, Menthyl Lactate, Pyrus Malus (Apple) Fruit Extract, Rosmarinus Officinalis (Rosemary) Leaf Extract, Sambucus Nigra (Elderberry) Fruit Extract, Sodium Lauryl Glucose Carboxylate.
- Questions?
- Atrix™ System
-
INGREDIENTS AND APPEARANCE
ATRIX SYSTEM 1
salicylic acid kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59088-713 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59088-713-00 1 in 1 KIT; Type 0: Not a Combination Product 10/25/2021 Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 1 TUBE 59 mL Part 2 1 BOTTLE 118 mL Part 1 of 2 ATRIX ACNE TREATMENT
salicylic acid creamProduct Information Item Code (Source) NDC:59088-446 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 20 mg in 1 mL Inactive Ingredients Ingredient Name Strength CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) WATER (UNII: 059QF0KO0R) GLUCOSAMINE HYDROCHLORIDE (UNII: 750W5330FY) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) CAPRYLYL GLYCOL (UNII: 00YIU5438U) STEARIC ACID (UNII: 4ELV7Z65AP) .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) DIMETHICONE (UNII: 92RU3N3Y1O) CETEARYL OLIVATE (UNII: 58B69Q84JO) OLIGOPEPTIDE-10 (UNII: Q46328TRNK) PHENOXYETHANOL (UNII: HIE492ZZ3T) DECYL GLUCOSIDE (UNII: Z17H97EA6Y) SACCHAROMYCES CEREVISIAE (UNII: 978D8U419H) SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR) UREA (UNII: 8W8T17847W) .ALPHA.-GLUCAN OLIGOSACCHARIDE (UNII: S95658MI3W) GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX) EDETATE DISODIUM (UNII: 7FLD91C86K) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) HEXYLENE GLYCOL (UNII: KEH0A3F75J) SODIUM HYDROXIDE (UNII: 55X04QC32I) GLYCERIN (UNII: PDC6A3C0OX) GLYCERYL STEARATE SE (UNII: FCZ5MH785I) DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5) SORBITAN OLIVATE (UNII: MDL271E3GR) PALMITIC ACID (UNII: 2V16EO95H1) LAMINARIA DIGITATA (UNII: 15E7C67EE8) ALLYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER (UNII: B9J55EA6QX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59088-446-05 59 mL in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 04/06/2021 Part 2 of 2 ATRIX ANTIBACTERIAL WASH
salicylic acid liquidProduct Information Item Code (Source) NDC:59088-445 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 20 mg in 1 mL Inactive Ingredients Ingredient Name Strength GRAPEFRUIT OIL (UNII: YR377U58W9) EDETATE DISODIUM (UNII: 7FLD91C86K) GLYCERIN (UNII: PDC6A3C0OX) MENTHYL LACTATE, (-)- (UNII: 2BF9E65L7I) APPLE (UNII: B423VGH5S9) ROSEMARY (UNII: IJ67X351P9) .ALPHA.-IONENE (UNII: B2ZN1K7W3Q) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) EUROPEAN ELDERBERRY (UNII: BQY1UBX046) WATER (UNII: 059QF0KO0R) CETYL HYDROXYETHYLCELLULOSE (350000 MW) (UNII: T7SWE4S2TT) LAURYL GLUCOSIDE (UNII: 76LN7P7UCU) MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) SODIUM LAURYL GLYCOL CARBOXYLATE (UNII: 8L0472VMYL) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59088-445-08 118 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 01/05/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 10/25/2021 Labeler - PureTek Corporation (785961046)