Label: NU-DERM SYSTEM NORMAL-OILY SKIN TRANSFORMATION- hydroquinone, homosalate, octisalate, and zinc oxide kit

  • NDC Code(s): 62032-531-00
  • Packager: OBAGI COSMECEUTICAL LLC
  • Category: HUMAN PRESCRIPTION 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 January 19, 2023

If you are a consumer or patient please visit this version.

  • SPL UNCLASSIFIED SECTION

    OBAGI NU-DERM®

    Rx only

    For external use only

  • DESCRIPTION

    Hydroquinone, USP 4% is 1, 4-benzenediol. The drug is freely soluble in water and in alcohol. Chemically, hydroquinone is designated as p-dihydroxybenzene; the empirical formula is C6H6O2; molecular weight is 110.11 g/mol. The chemical structure is in the diagram below.

    Chemical Structure

    C6H6O2

    Each gram of Obagi Nu-Derm® Clear contains:

    ACTIVE: Hydroquinone, USP 4% (40 mg/g)

    INACTIVES: ascorbic acid, BHT, butylparaben, cetyl alcohol, disodium EDTA, glycerin, lactic acid, methylparaben, propylparaben, saponins, sodium lauryl sulfate, sodium metabisulfite, stearyl alcohol, tocopheryl acetate, water (aqua)

    Each gram of Obagi Nu-Derm Blender® contains:

    ACTIVE: Hydroquinone, USP 4% (40 mg/g)

    INACTIVES: ascorbic acid, BHT, cetyl alcohol, disodium EDTA, glycerin, lactic acid, methylparaben, phenyl trimethicone, PPG-2 myristyl ether propionate, propylparaben, saponins, sodium lauryl sulfate, sodium metabisulfite, TEA-salicylate, tocopheryl acetate, water (aqua)

    Each gram of Obagi Nu-Derm® Sunfader® contains:

    ACTIVES: Hydroquinone, USP 4% (40mg/g); Octinoxate, USP 7.5%; Oxybenzone, USP 5.5%

    INACTIVES: ascorbic acid, BHT, butylparaben, cetyl alcohol, disodium EDTA, glycerin, methylparaben, propylparaben, saponins, sodium lauryl sulfate, sodium metabisulfite, stearyl alcohol, tocopheryl acetate, water (aqua)

  • CLINICAL PHARMACOLOGY

    Topical application of hydroquinone produces a reversible depigmentation of the skin by inhibition of the enzymatic oxidation of tyrosine to 3, 4-dihydroxyphenylalanine (DOPA) and suppression of other melanocyte metabolic processes. Exposure to sunlight or ultraviolet light will cause repigmentation of the bleached areas, which may be prevented by the use of sunscreen agents such as those contained in Obagi Nu-Derm Sunfader® and Obagi Nu-Derm® Sun Shield Matte Broad Spectrum SPF 50.

  • INDICATIONS AND USAGE

    For the gradual bleaching of hyperpigmented skin conditions such as chloasma, melasma, freckles, senile lentigines and other unwanted areas of melanin hyperpigmentation.

  • CONTRAINDICATIONS

    People with prior history of sensitivity or allergic reaction to this product or any of its ingredients should not use it. The safety of topical hydroquinone use during pregnancy or in children (12 years and under) has not been established.

  • WARNINGS

    Hydroquinone is a skin bleaching agent, which may produce unwanted cosmetic effects if not used as directed. The physician should be familiar with the contents of this insert before prescribing or dispensing this product.

    Test for skin sensitivity before using by applying a small amount to an unbroken patch of skin and check within 24 hours. Some users of this product may experience a mild skin irritation. If skin irritation becomes severe, stop use and consult a doctor. Close patient supervision is recommended.

  • WARNINGS

    Avoid contact with eyes, nose, mouth and lips. In case of accidental contact, patient should rinse thoroughly with water and contact a physician. Sunscreen use is an essential aspect of hydroquinone therapy because even minimal sunlight exposure sustains melanocytic activity.

    Contains sodium metabisulfite, a sulfite that may cause allergic-type reactions including anaphylactic symptoms and life-threatening or less severe asthmatic episodes in certain susceptible people. The overall prevalence of sulfite sensitivity in the general population is unknown and probably low. Sulfite sensitivity is seen more frequently in asthmatic than in nonasthmatic people.

  • PRECAUTIONS

    (also see WARNINGS):

    Treatment should be limited to relatively small areas of the body at one time since some patients experience a transient skin reddening and a mild burning sensation, which does not preclude treatment.

    PREGNANCY CATEGORY C

    Animal reproduction studies have not been conducted with topical hydroquinone. It is also not known whether hydroquinone can cause fetal harm when used topically on a pregnant woman or affect reproductive capacity. It is not known to what degree, if any, topical hydroquinone is absorbed systemically. Topical hydroquinone should be used on pregnant women only when clearly indicated.

    NURSING MOTHERS

    It is not known whether topical hydroquinone is absorbed or excreted in human milk. Caution is advised when topical hydroquinone is used by a nursing mother.

    PEDIATRIC USAGE

    Safety and effectiveness in children below the age of 12 years have not been established.

  • ADVERSE REACTIONS

    No systemic adverse reactions have been reported. Occasional hypersensitivity (localized contact dermatitis) may occur, in which case the product should be discontinued and the physician notified immediately.

    To report SUSPECTED ADVERSE REACTIONS, contact Obagi Cosmeceuticals LLC, at 1-800-636-7546 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.

  • DOSAGE AND ADMINISTRATION

    A thin application should be applied once or twice daily or as directed by a physician. If no improvement is seen after three (3) months of treatment, use of this product should be discontinued. Sun exposure should be limited by using a sunscreen agent or protective clothing to cover bleached skin when using and after using this product in order to prevent darkening from reoccurring.

  • HOW SUPPLIED

    Obagi Nu-Derm® Clear is available as follows:

    Net wt. 2 oz. (57 g) bottle
    NDC 62032-101-36

    Obagi Nu-Derm Blender® is available as follows:

    Net wt. 2 oz. (57 g) bottle
    NDC 62032-100-36

    Net wt. 1 oz. (28 g) bottle
    NDC 62032-100-10

    Obagi Nu-Derm Sunfader® is available as follows:

    Net wt. 2 oz. (57 g) bottle
    NDC 62032-116-36

    Store at controlled room temperature: 15° to 25°C (59° to 77°F). Keep out of direct sunlight.

  • SPL UNCLASSIFIED SECTION

    Image1-800-636-7546

    Manufactured for:
    Obagi Cosmeceuticals LLC,
    Long Beach, CA 90806

    All products/brand names, whether designated by notice or not (®/TM), are trademarks of Obagi Cosmeceuticals LLC and/or its affiliates.

    ©2019 Obagi Cosmeceuticals LLC.
    All rights reserved.   www.obagi.com

    Revised 01/2019   9458404

    Obagi Nu-Derm® Clear (Hydroquinone, USP 4%)
    Skin Bleaching Cream

    Obagi Nu-Derm Blender® (Hydroquinone, USP 4%)
    Skin Bleaching Cream

    Obagi Nu-Derm Sunfader®
    (Hydroquinone, USP 4%; Octinoxate, USP 7.5%; Oxybenzone, USP 5.5%) Skin Bleaching Cream with Sunscreens

  • SPL UNCLASSIFIED SECTION

    Sun Shield Matte Broad Spectrum SPF 50
    Net wt. 3 oz. (85 g) AM

    Drug Facts

  • ACTIVE INGREDIENT

    Active ingredientsPurpose
    Homosalate 10%Sunscreen
    Octisalate 5%Sunscreen
    Zinc Oxide 16.5%Sunscreen
  • Uses

    • helps prevent sunburn
    • If used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun
  • Warnings

    For external use only

    Do not use on damaged or broken skin

    Stop use and ask a doctor if rash occurs

    When using this product keep out of eyes. Rinse with water to remove.

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • apply liberally 15 minutes before sun exposure
    • use a water resistant sunscreen if swimming or sweating
    • reapply at least every 2 hours
    • Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including:
      • limit time in the sun, especially from 10 a.m.–2 p.m.
      • wear long-sleeved shirts, pants, hats, and sunglasses
    • children under 6 months: Ask a doctor
  • Other information

    • store at controlled room temperature: 15°C–25°C (59°F–77°F)
    • protect this product from excessive heat and direct sun
  • Inactive ingredients

    Water (Aqua), C15-19 Alkane, Octyldodecyl Neopentanoate, Polymethylsilsesquioxane, Sorbitan Olivate, Silica, Polyglyceryl-6 Polyrininoleate, Sodium Chloride, Xanthan Gum, Glycerin, Hydroxyacetophenone, Disodium EDTA, 1,2-Hexanediol, Caprylyl Glycol, Sodium Hydroxide, Triethoxycaprylsilane, Polyhydroxystearic Acid, Disteardimonium Hectorite, Polyglyceryl-2 Isostearate, Euphorbia Cerifera (candelilla) Wax, Beeswax, Dimethicone

  • Questions or comments?

    1.800.636.7546

    Monday–Friday 9 a.m.– 4 p.m. Pacific Time

  • SPL UNCLASSIFIED SECTION

    Distributed by Obagi Cosmeceuticals LLC, Long Beach, CA 90806

  • PRINCIPAL DISPLAY PANEL - Kit Carton

    NDC# 62032-531-00

    OBAGI®
    MEDICAL

    OBAGI NU-DERM® SYSTEM

    NORMAL OILY

    Skin Transformation Kit

    Principal Display Panel - Kit Carton
  • INGREDIENTS AND APPEARANCE
    NU-DERM SYSTEM NORMAL-OILY   SKIN TRANSFORMATION
    hydroquinone, homosalate, octisalate, and zinc oxide kit
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:62032-531
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:62032-531-001 in 1 CARTON12/02/2019
    Quantity of Parts
    Part #Package QuantityTotal Product Quantity
    Part 11 BOTTLE, PLASTIC 57 g
    Part 21 BOTTLE, PLASTIC 198 mL
    Part 31 BOTTLE, PLASTIC 198 mL
    Part 41 BOTTLE, PLASTIC 57 g
    Part 51 BOTTLE, PLASTIC 48 g
    Part 61 BOTTLE, PLASTIC 57 g
    Part 71 TUBE 85 g
    Part 1 of 7
    OBAGI NU-DERM EXFODERM FORTE 
    face and neck (excluding shaving preparations) lotion
    Product Information
    Route of AdministrationTOPICAL
    Other Ingredients
    Ingredient KindIngredient NameQuantity
    INGRWATER (UNII: 059QF0KO0R)  
    INGRGLYCERIN (UNII: PDC6A3C0OX)  
    INGRDIMETHICONE (UNII: 92RU3N3Y1O)  
    INGRMETHYLPARABEN (UNII: A2I8C7HI9T)  
    INGRPROPYLPARABEN (UNII: Z8IX2SC1OH)  
    INGRPOLYSORBATE 60 (UNII: CAL22UVI4M)  
    INGRTROLAMINE (UNII: 9O3K93S3TK)  
    INGRMEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
    INGRCETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    INGRCETYL ALCOHOL (UNII: 936JST6JCN)  
    INGRLACTIC ACID, UNSPECIFIED FORM (UNII: 33X04XA5AT)  
    INGREMU OIL (UNII: 344821WD61)  
    INGRSTEARIC ACID (UNII: 4ELV7Z65AP)  
    INGRSTEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
    INGRGlycolic Acid (UNII: 0WT12SX38S)  
    Product Characteristics
    colorWHITEC48325
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    157 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    COSMETIC01/01/1988
    Part 2 of 7
    OBAGI NU-DERM FOAMING 
    cleansing (cold creams, cleansing lotions, liquids, and pads) gel
    Product Information
    Route of AdministrationTOPICAL
    Other Ingredients
    Ingredient KindIngredient NameQuantity
    INGRWATER (UNII: 059QF0KO0R)  
    INGRPHENOXYETHANOL (UNII: HIE492ZZ3T)  
    INGRMETHYLPARABEN (UNII: A2I8C7HI9T)  
    INGRPROPYLPARABEN (UNII: Z8IX2SC1OH)  
    INGRBUTYLPARABEN (UNII: 3QPI1U3FV8)  
    INGRETHYLPARABEN (UNII: 14255EXE39)  
    INGRISOBUTYLPARABEN (UNII: 0QQJ25X58G)  
    INGRFD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    INGRSODIUM LAUROYL OAT AMINO ACIDS (UNII: FSW2K9B9N5)  
    INGRCOCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    INGRSODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)  
    INGRALOE VERA LEAF (UNII: ZY81Z83H0X)  
    INGRSODIUM CHLORIDE (UNII: 451W47IQ8X)  
    INGRMEDICAGO SATIVA WHOLE (UNII: DJO934BRBD)  
    INGRCHAMOMILE (UNII: FGL3685T2X)  
    INGRXANTHAN GUM (UNII: TTV12P4NEE)  
    INGRD&C RED NO. 33 (UNII: 9DBA0SBB0L)  
    Product Characteristics
    colorREDC48326
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1198 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    COSMETIC01/01/1988
    Part 3 of 7
    OBAGI NU-DERM TONER 
    cleansing (cold creams, cleansing lotions, liquids, and pads) liquid
    Product Information
    Route of AdministrationTOPICAL
    Other Ingredients
    Ingredient KindIngredient NameQuantity
    INGRWATER (UNII: 059QF0KO0R)  
    INGRGLYCERIN (UNII: PDC6A3C0OX)  
    INGRHAMAMELIS VIRGINIANA TOP WATER (UNII: NT00Y05A2V)  
    INGRSODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)  
    INGRDMDM HYDANTOIN (UNII: BYR0546TOW)  
    INGRIODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)  
    INGRPOTASSIUM ALUM (UNII: 1L24V9R23S)  
    INGRPANTHENOL (UNII: WV9CM0O67Z)  
    INGRSAGE (UNII: 065C5D077J)  
    INGRCALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)  
    INGRPOLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    INGRALLANTOIN (UNII: 344S277G0Z)  
    INGRALOE VERA LEAF (UNII: ZY81Z83H0X)  
    INGRFD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    Product Characteristics
    colorBLUEC48333
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1198 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    COSMETIC01/02/1988
    Part 4 of 7
    NU-DERM CLEAR   SKIN BLEACHING AND CORRECTOR
    hydroquinone cream
    Product Information
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HYDROQUINONE (UNII: XV74C1N1AE) (HYDROQUINONE - UNII:XV74C1N1AE) HYDROQUINONE40 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    BUTYLPARABEN (UNII: 3QPI1U3FV8)  
    STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    LACTIC ACID, UNSPECIFIED FORM (UNII: 33X04XA5AT)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    ASCORBIC ACID (UNII: PQ6CK8PD0R)  
    SODIUM METABISULFITE (UNII: 4VON5FNS3C)  
    WATER (UNII: 059QF0KO0R)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
    Product Characteristics
    ColorWHITEScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    157 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    UNAPPROVED DRUG OTHER01/01/1988
    Part 5 of 7
    OBAGI NU-DERM HYDRATE   FACIAL MOISTURIZER
    face and neck (excluding shaving preparations)
    Product Information
    Route of AdministrationTOPICAL
    Other Ingredients
    Ingredient KindIngredient NameQuantity
    INGRWATER (UNII: 059QF0KO0R)  
    INGRGLYCERIN (UNII: PDC6A3C0OX)  
    INGRMEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
    INGRSODIUM HYDROXIDE (UNII: 55X04QC32I)  
    INGRCAESALPINIA SPINOSA RESIN (UNII: WL3883U2PO)  
    INGRSHEA BUTTER (UNII: K49155WL9Y)  
    INGRDIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)  
    INGRCYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    INGRCETYL ALCOHOL (UNII: 936JST6JCN)  
    INGRSACCHARIDE ISOMERATE (UNII: W8K377W98I)  
    INGRDIMETHICONE (UNII: 92RU3N3Y1O)  
    INGRTOCOPHEROL (UNII: R0ZB2556P8)  
    INGRLAURETH-12 (UNII: OAH19558U1)  
    INGRPHENOXYETHANOL (UNII: HIE492ZZ3T)  
    INGRETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    INGRSTEARIC ACID (UNII: 4ELV7Z65AP)  
    INGRAVOCADO OIL (UNII: 6VNO72PFC1)  
    INGRSOY STEROL (UNII: PL360EPO9J)  
    INGRCAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    INGRLEVOMENOL (UNII: 24WE03BX2T)  
    INGRHEXYLENE GLYCOL (UNII: KEH0A3F75J)  
    INGRTETRAHYDRODIFERULOYLMETHANE (UNII: 00U0645U03)  
    INGRPANTHENOL (UNII: WV9CM0O67Z)  
    INGRMANGIFERA INDICA SEED BUTTER (UNII: 4OXD9M35X2)  
    INGRSODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024)  
    INGRCARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    INGRALLANTOIN (UNII: 344S277G0Z)  
    INGRGLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    Product Characteristics
    colorWHITEC48325
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    148 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    COSMETIC11/07/2012
    Part 6 of 7
    NU-DERM BLENDER   SKIN LIGHTENER AND BLENDING
    hydroquinone cream
    Product Information
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HYDROQUINONE (UNII: XV74C1N1AE) (HYDROQUINONE - UNII:XV74C1N1AE) HYDROQUINONE40 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    PPG-2 MYRISTYL ETHER PROPIONATE (UNII: 88R97D8U8A)  
    TROLAMINE SALICYLATE (UNII: H8O4040BHD)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    LACTIC ACID, UNSPECIFIED FORM (UNII: 33X04XA5AT)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    ASCORBIC ACID (UNII: PQ6CK8PD0R)  
    SODIUM METABISULFITE (UNII: 4VON5FNS3C)  
    WATER (UNII: 059QF0KO0R)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
    PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)  
    Product Characteristics
    ColorWHITEScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    157 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    UNAPPROVED DRUG OTHER01/01/1988
    Part 7 of 7
    NU-DERM SUN SHIELD MATTE BROAD SPECTRUM SPF 50   SUNSCREEN
    homosalate, octisalate, and zinc oxide lotion
    Product Information
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE100 mg  in 1 g
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE50 mg  in 1 g
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE165 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    Hydroxyacetophenone (UNII: G1L3HT4CMH)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    Sodium Chloride (UNII: 451W47IQ8X)  
    Sodium Hydroxide (UNII: 55X04QC32I)  
    Octyldodecyl Neopentanoate (UNII: X8725R883T)  
    Triethoxycaprylylsilane (UNII: LDC331P08E)  
    C15-19 Alkane (UNII: CI87N1IM01)  
    Disteardimonium Hectorite (UNII: X687XDK09L)  
    POLYGLYCERYL-2 ISOSTEARATE (UNII: 7B8OE71MQC)  
    Sorbitan Olivate (UNII: MDL271E3GR)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    1,2-HEXANEDIOL (UNII: TR046Y3K1G)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    CANDELILLA WAX (UNII: WL0328HX19)  
    Yellow Wax (UNII: 2ZA36H0S2V)  
    POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69)  
    Silicon Dioxide (UNII: ETJ7Z6XBU4)  
    Product Characteristics
    ColorWHITEScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    185 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC MONOGRAPH FINALpart35212/02/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    UNAPPROVED DRUG OTHER12/02/2019
    Labeler - OBAGI COSMECEUTICAL LLC (790553353)
    Establishment
    NameAddressID/FEIBusiness Operations
    PURETEK CORPORATION785961046MANUFACTURE(62032-531) , LABEL(62032-531) , PACK(62032-531)
    Establishment
    NameAddressID/FEIBusiness Operations
    G.S. COSMECEUTICAL USA, INC.017014734MANUFACTURE(62032-531)
    Establishment
    NameAddressID/FEIBusiness Operations
    Swiss-American CDMO, LLC080170933MANUFACTURE(62032-531)