NU-DERM SUNFADER

Manufacturer
Obagi Cosmeceuticals LLC | G.S.COSMECEUTICAL USA, INC.
Effective date
2025-01-01
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
10
Source
full-release
Hydrated at
2026-05-31 21:27:29

Label at a glance#

ProductNU-DERM CLEAR Skin Bleaching and Corrector
Active ingredientHYDROQUINONE, OCTINOXATE, OXYBENZONE
Label structure14 sections

Indications and uses

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

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, a sunblocking agent, or protective clothing to cover bleached skin when using and after using this product in order to prevent darkening from reoccurring.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Rx Only

For external use only

DESCRIPTION

DESCRIPTION SECTION

Hydroquinone is 1, 4-benzenediol. The drug is freely soluble in water and in alcohol. Chemically, hydroquinone is designed 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
Chemical Structure

Each gram of Obagi Nu-Derm Clear contains:

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

Inactive ingredients: water, cetyl alcohol, glycerin, sodium lauryl sulfate, stearyl alcohol, lactic acid, tocopheryl acetate, ascorbic acid, sodium metabisulfite, disodium EDTA, methylparaben, BHT, propylparaben, saponins, butylparaben

Each gram of Obagi Nu-Derm Blender contains:

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

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

Each gram of Obagi Nu-Derm Sunfader contains:

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

Inactive ingredients: water, cetyl alcohol, glycerin, sodium lauryl sulfate, stearyl alcohol, tocopheryl acetate, ascorbic acid, sodium metabisulfite, disodium EDTA, methylparaben, BHT, saponins, propylparaben, butylparaben

CLINICAL PHARMACOLOGY

CLINICAL PHARMACOLOGY SECTION

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 sunblocking agents or sunscreen agents contained in Obagi Nu-Derm Sunfader and Obagi Nu-Derm Sun Shield Matte Broad Spectrum SPF 50.

INDICATIONS AND USAGE

INDICATIONS & USAGE SECTION

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

CONTRAINDICATIONS

CONTRAINDICATIONS SECTION

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

WARNINGS SECTION

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. Minor redness is not a contraindication, but where there is itching or vesicle formation or excessive inflammatory response, product should be discontinued and physician consulted. 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

PRECAUTIONS SECTION

(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

PREGNANCY SECTION

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

NURSING MOTHERS SECTION

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

PEDIATRIC USE SECTION

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

ADVERSE REACTIONS

ADVERSE REACTIONS SECTION

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.

DOSAGE AND ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

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, a sunblocking agent, or protective clothing to cover bleached skin when using and after using this product in order to prevent darkening from reoccurring.

HOW SUPPLIED

HOW SUPPLIED SECTION

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

STORAGE AND HANDLING SECTION

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

SPL UNCLASSIFIED SECTION

⍰ 1-800-636-7546

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

©2018 Obagi Cosmeceuticals LLC.
All rights reserved.
www.obagi.com

Revised 03/2018
9458403

PRINCIPAL DISPLAY PANEL - 57 g Bottle Label - 3

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

OBAGI

NU-DERM®
NDC 62032-101-36

AM CLEAR
PM
3

SKIN BLEACHING
& CORRECTOR CREAM

HYDROQUINONE USP, 4%
Rx ONLY

Net wt. 2 oz. (57g)

PRINCIPAL DISPLAY PANEL - 57 g Bottle Label - 3
PRINCIPAL DISPLAY PANEL - 57 g Bottle Label - 3

PRINCIPAL DISPLAY PANEL - 57 g Bottle Label - 5

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

OBAGI

NU-DERM®
NDC 62032-100-36

BLENDER®

PM
5

SKIN LIGHTENER
& BLENDING CREAM

HYDROQUINONE USP, 4%
Rx ONLY

Net wt. 2 oz. (57g)

PRINCIPAL DISPLAY PANEL - 57 g Bottle Label - 5
PRINCIPAL DISPLAY PANEL - 57 g Bottle Label - 5

PRINCIPAL DISPLAY PANEL - 57 g Bottle Label - 6

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

OBAGI

NU-DERM®
NDC 62032-116-36

AM
6

SUNFADER®
HYDROQUINONE USP, 4%

SKIN LIGHTENER
WITH SUNSCREEN
(SPF 15) PABA-FREE

Rx only

Net wt. 2 oz. (57 g)

PRINCIPAL DISPLAY PANEL - 57 g Bottle Label - 6
PRINCIPAL DISPLAY PANEL - 57 g Bottle Label - 6

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
197795hydroquinone 4 % Topical CreamPSN10
197795hydroquinone 40 MG/ML Topical CreamSCD10
197795hydroquinone 4 % Topical CreamSY10

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
HYDROQUINONE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
85490a6b-2306-6bf2-c51b-eb63537dc2daProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
62032-100-102025-03-11C16284748780-12cef2736-8bc5-d83d-e063-dadaa90ab31fObagi 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
62032-100-362025-03-11C16284748780-12cef2736-8bc5-d83d-e063-dadaa90ab31fObagi 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
62032-101-362025-03-11C16284748780-12cef2736-8bc5-d83d-e063-dadaa90ab31fObagi 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
62032-116-362025-03-11C16284748780-12cef2736-8bc5-d83d-e063-dadaa90ab31fObagi 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
62032-100-102025-01-30C16284748780-12cef2736-8bc5-d83d-e063-dadaa90ab31fObagi 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
62032-100-362025-01-30C16284748780-12cef2736-8bc5-d83d-e063-dadaa90ab31fObagi 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
62032-101-362025-01-30C16284748780-12cef2736-8bc5-d83d-e063-dadaa90ab31fObagi 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
62032-116-362025-01-30C16284748780-12cef2736-8bc5-d83d-e063-dadaa90ab31fObagi 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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62032-100-10NU-DERM BLENDERSkin Lightener and Blending28 g in 1 BOTTLE, PLASTICCREAM2810
62032-100-36NU-DERM BLENDERSkin Lightener and Blending57 g in 1 BOTTLE, PLASTICCREAM5710
62032-101-36NU-DERM CLEARSkin Bleaching and Corrector57 g in 1 BOTTLE, PLASTICCREAM5710
62032-116-36NU-DERM SUNFADERSkin Lightener with Sunscreen (SPF 15) PABA FREE57 g in 1 BOTTLE, PLASTICLOTION5710

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62032-100NU-DERM CLEAR SKIN BLEACHING AND CORRECTOR (HYDROQUINONE) CREAM NU-DERM BLENDER SKIN LIGHTENER AND BLENDING (HYDROQUINONE) CREAM NU-DERM SUNFADER SKIN LIGHTENER WITH SUNSCREEN (SPF 15) PABA FREE (HYDROQUINONE, OCTINOXATE, AND OXYBENZONE) LOTION [OBAGI COSMECEUTICALS LLC]10Current NDC, Legacy NDC, 2 package rows20250315_e5c450af-958e-41e3-9c2f-fda76b3596f5.zip
62032-101NU-DERM CLEAR SKIN BLEACHING AND CORRECTOR (HYDROQUINONE) CREAM NU-DERM BLENDER SKIN LIGHTENER AND BLENDING (HYDROQUINONE) CREAM NU-DERM SUNFADER SKIN LIGHTENER WITH SUNSCREEN (SPF 15) PABA FREE (HYDROQUINONE, OCTINOXATE, AND OXYBENZONE) LOTION [OBAGI COSMECEUTICALS LLC]10Current NDC, Legacy NDC, 1 package rows20250315_e5c450af-958e-41e3-9c2f-fda76b3596f5.zip
62032-116NU-DERM CLEAR SKIN BLEACHING AND CORRECTOR (HYDROQUINONE) CREAM NU-DERM BLENDER SKIN LIGHTENER AND BLENDING (HYDROQUINONE) CREAM NU-DERM SUNFADER SKIN LIGHTENER WITH SUNSCREEN (SPF 15) PABA FREE (HYDROQUINONE, OCTINOXATE, AND OXYBENZONE) LOTION [OBAGI COSMECEUTICALS LLC]10Current NDC, Legacy NDC, 1 package rows20250315_e5c450af-958e-41e3-9c2f-fda76b3596f5.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
HYDROQUINONEACTIVE INGREDIENTXV74C1N1AE3
OCTINOXATEACTIVE INGREDIENT4Y5P7MUD513
OXYBENZONEACTIVE INGREDIENT95OOS7VE0Y3
HYDROQUINONEACTIVE MOIETYXV74C1N1AE3
OCTINOXATEACTIVE MOIETY4Y5P7MUD513
OXYBENZONEACTIVE MOIETY95OOS7VE0Y3
.ALPHA.-TOCOPHEROL ACETATEINACTIVE INGREDIENT9E8X80D2L03
ASCORBIC ACIDINACTIVE INGREDIENTPQ6CK8PD0R3
BUTYLATED HYDROXYTOLUENEINACTIVE INGREDIENT1P9D0Z171K3
BUTYLPARABENINACTIVE INGREDIENT3QPI1U3FV83
CETYL ALCOHOLINACTIVE INGREDIENT936JST6JCN3
EDETATE DISODIUMINACTIVE INGREDIENT7FLD91C86K3
GLYCERININACTIVE INGREDIENTPDC6A3C0OX3
LACTIC ACIDINACTIVE INGREDIENT33X04XA5AT3
METHYLPARABENINACTIVE INGREDIENTA2I8C7HI9T3
PHENYL TRIMETHICONEINACTIVE INGREDIENTDR0K5NOJ4R3
PPG-2 MYRISTYL ETHER PROPIONATEINACTIVE INGREDIENT88R97D8U8A3
PROPYLPARABENINACTIVE INGREDIENTZ8IX2SC1OH3
SODIUM LAURYL SULFATEINACTIVE INGREDIENT368GB5141J3
SODIUM METABISULFITEINACTIVE INGREDIENT4VON5FNS3C3
STEARYL ALCOHOLINACTIVE INGREDIENT2KR89I4H1Y3
TROLAMINE SALICYLATEINACTIVE INGREDIENTH8O4040BHD3
WATERINACTIVE INGREDIENT059QF0KO0R3

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 24 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62032-10062032-100-10, 62032-100-36
62032-10162032-101-36
62032-11662032-116-36

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 2 · 47 matching rows.

Source Document#

Source XML · Source PDF

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 2 · 112 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
LACTIC ACIDLACTIC ACID33X04XA5ATCREAM / TOPICAL1 %w/wExact identifier — unii+route+dosage form
7 equally ranked IID candidates
PROPYLPARABENPROPYLPARABENZ8IX2SC1OHLOTION / TOPICAL140 mgExact identifier — unii+route+dosage form
7 equally ranked IID candidates
SODIUM LAURYL SULFATESODIUM LAURYL SULFATE368GB5141JCREAM / TOPICAL214 mgExact identifier — unii+route+dosage form
7 equally ranked IID candidates
BUTYLPARABENBUTYLPARABEN3QPI1U3FV8LOTION / TOPICAL4 mgExact identifier — unii+route+dosage form
7 equally ranked IID candidates
.ALPHA.-TOCOPHEROL ACETATE.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0FILM / BUCCAL0.09 mgExact identifier — unii candidate
21 equally ranked IID candidates
CETYL ALCOHOLCETYL ALCOHOL936JST6JCNCREAM / TOPICAL1280 mgExact identifier — unii+route+dosage form
7 equally ranked IID candidates
CETYL ALCOHOLCETYL ALCOHOL936JST6JCNCREAM / TOPICAL1280 mgExact identifier — unii+route+dosage form
7 equally ranked IID candidates
LACTIC ACIDLACTIC ACID33X04XA5ATCREAM / TOPICAL1 %w/wExact identifier — unii+route+dosage form
7 equally ranked IID candidates
BUTYLATED HYDROXYTOLUENEBUTYLATED HYDROXYTOLUENE1P9D0Z171KCREAM / TOPICAL6 mgExact identifier — unii+route+dosage form
7 equally ranked IID candidates
PROPYLPARABENPROPYLPARABENZ8IX2SC1OHCREAM / TOPICAL6 mgExact identifier — unii+route+dosage form
7 equally ranked IID candidates
.ALPHA.-TOCOPHEROL ACETATE.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0TABLET / ORAL0.5 mgExact identifier — unii candidate
21 equally ranked IID candidates
ASCORBIC ACIDASCORBIC ACIDPQ6CK8PD0RGEL / TOPICAL7 mgExact identifier — unii+route
14 equally ranked IID candidates
GLYCERINGLYCERINPDC6A3C0OXCREAM / TOPICAL1720 mgExact identifier — unii+route+dosage form
7 equally ranked IID candidates
EDETATE DISODIUMEDETATE DISODIUM7FLD91C86KLOTION / TOPICAL22 mgExact identifier — unii+route+dosage form
7 equally ranked IID candidates
BUTYLATED HYDROXYTOLUENEBUTYLATED HYDROXYTOLUENE1P9D0Z171KCREAM / TOPICAL6 mgExact identifier — unii+route+dosage form
7 equally ranked IID candidates
.ALPHA.-TOCOPHEROL ACETATE.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0FILM / BUCCAL0.09 mgExact identifier — unii candidate
21 equally ranked IID candidates
SODIUM METABISULFITESODIUM METABISULFITE4VON5FNS3CCREAM / TOPICAL0.2 %w/wExact identifier — unii+route+dosage form
7 equally ranked IID candidates
ASCORBIC ACIDASCORBIC ACIDPQ6CK8PD0RSOLUTION / TOPICAL0.04 %w/wExact identifier — unii+route
14 equally ranked IID candidates
BUTYLATED HYDROXYTOLUENEBUTYLATED HYDROXYTOLUENE1P9D0Z171KCREAM / TOPICAL6 mgExact identifier — unii+route+dosage form
7 equally ranked IID candidates
BUTYLATED HYDROXYTOLUENEBUTYLATED HYDROXYTOLUENE1P9D0Z171KLOTION / TOPICAL1000 mgExact identifier — unii+route+dosage form
7 equally ranked IID candidates
BUTYLATED HYDROXYTOLUENEBUTYLATED HYDROXYTOLUENE1P9D0Z171KCREAM / TOPICAL6 mgExact identifier — unii+route+dosage form
7 equally ranked IID candidates
LACTIC ACIDLACTIC ACID33X04XA5ATCREAM / TOPICAL1 %w/wExact identifier — unii+route+dosage form
7 equally ranked IID candidates
STEARYL ALCOHOLSTEARYL ALCOHOL2KR89I4H1YCREAM / TOPICAL162000 mgExact identifier — unii+route+dosage form
7 equally ranked IID candidates
GLYCERINGLYCERINPDC6A3C0OXCREAM / TOPICAL1720 mgExact identifier — unii+route+dosage form
7 equally ranked IID candidates
SODIUM LAURYL SULFATESODIUM LAURYL SULFATE368GB5141JCREAM / TOPICAL214 mgExact identifier — unii+route+dosage form
7 equally ranked IID candidates
STEARYL ALCOHOLSTEARYL ALCOHOL2KR89I4H1YLOTION / TOPICAL1140 mgExact identifier — unii+route+dosage form
7 equally ranked IID candidates
SODIUM LAURYL SULFATESODIUM LAURYL SULFATE368GB5141JCREAM / TOPICAL214 mgExact identifier — unii+route+dosage form
7 equally ranked IID candidates
SODIUM LAURYL SULFATESODIUM LAURYL SULFATE368GB5141JLOTION / TOPICAL111 mgExact identifier — unii+route+dosage form
7 equally ranked IID candidates
SODIUM METABISULFITESODIUM METABISULFITE4VON5FNS3CCREAM / TOPICAL0.2 %w/wExact identifier — unii+route+dosage form
7 equally ranked IID candidates
PROPYLPARABENPROPYLPARABENZ8IX2SC1OHCREAM / TOPICAL6 mgExact identifier — unii+route+dosage form
7 equally ranked IID candidates
CETYL ALCOHOLCETYL ALCOHOL936JST6JCNCREAM / TOPICAL1280 mgExact identifier — unii+route+dosage form
7 equally ranked IID candidates
BUTYLPARABENBUTYLPARABEN3QPI1U3FV8CREAM / TOPICAL0.4 %w/wExact identifier — unii+route+dosage form
7 equally ranked IID candidates
.ALPHA.-TOCOPHEROL ACETATE.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0TABLET / ORAL0.5 mgExact identifier — unii candidate
21 equally ranked IID candidates
.ALPHA.-TOCOPHEROL ACETATE.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0TABLET / ORAL0.5 mgExact identifier — unii candidate
21 equally ranked IID candidates
EDETATE DISODIUMEDETATE DISODIUM7FLD91C86KCREAM / TOPICAL14 mgExact identifier — unii+route+dosage form
7 equally ranked IID candidates
GLYCERINGLYCERINPDC6A3C0OXCREAM / TOPICAL1720 mgExact identifier — unii+route+dosage form
7 equally ranked IID candidates
EDETATE DISODIUMEDETATE DISODIUM7FLD91C86KCREAM / TOPICAL14 mgExact identifier — unii+route+dosage form
7 equally ranked IID candidates
GLYCERINGLYCERINPDC6A3C0OXLOTION / TOPICAL3990 mgExact identifier — unii+route+dosage form
7 equally ranked IID candidates
ASCORBIC ACIDASCORBIC ACIDPQ6CK8PD0RSOLUTION / TOPICAL0.04 %w/wExact identifier — unii+route
14 equally ranked IID candidates
SODIUM LAURYL SULFATESODIUM LAURYL SULFATE368GB5141JCREAM / TOPICAL214 mgExact identifier — unii+route+dosage form
7 equally ranked IID candidates
LACTIC ACIDLACTIC ACID33X04XA5ATLOTION / TOPICAL5.7 %w/wExact identifier — unii+route+dosage form
7 equally ranked IID candidates
.ALPHA.-TOCOPHEROL ACETATE.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0CAPSULE / ORAL2 mgExact identifier — unii candidate
21 equally ranked IID candidates
CETYL ALCOHOLCETYL ALCOHOL936JST6JCNCREAM / TOPICAL1280 mgExact identifier — unii+route+dosage form
7 equally ranked IID candidates
BUTYLPARABENBUTYLPARABEN3QPI1U3FV8LOTION / TOPICAL4 mgExact identifier — unii+route+dosage form
7 equally ranked IID candidates
METHYLPARABENMETHYLPARABENA2I8C7HI9TLOTION / TOPICAL351 mgExact identifier — unii+route+dosage form
7 equally ranked IID candidates
GLYCERINGLYCERINPDC6A3C0OXCREAM / TOPICAL1720 mgExact identifier — unii+route+dosage form
7 equally ranked IID candidates
.ALPHA.-TOCOPHEROL ACETATE.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0FILM / BUCCAL0.09 mgExact identifier — unii candidate
21 equally ranked IID candidates
GLYCERINGLYCERINPDC6A3C0OXLOTION / TOPICAL3990 mgExact identifier — unii+route+dosage form
7 equally ranked IID candidates
SODIUM METABISULFITESODIUM METABISULFITE4VON5FNS3CCREAM / TOPICAL0.2 %w/wExact identifier — unii+route+dosage form
7 equally ranked IID candidates
.ALPHA.-TOCOPHEROL ACETATE.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0FILM / BUCCAL0.09 mgExact identifier — unii candidate
21 equally ranked IID candidates
METHYLPARABENMETHYLPARABENA2I8C7HI9TCREAM / TOPICAL3000 mgExact identifier — unii+route+dosage form
7 equally ranked IID candidates
.ALPHA.-TOCOPHEROL ACETATE.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0CAPSULE / ORAL2 mgExact identifier — unii candidate
21 equally ranked IID candidates
STEARYL ALCOHOLSTEARYL ALCOHOL2KR89I4H1YCREAM / TOPICAL162000 mgExact identifier — unii+route+dosage form
7 equally ranked IID candidates
METHYLPARABENMETHYLPARABENA2I8C7HI9TCREAM / TOPICAL3000 mgExact identifier — unii+route+dosage form
7 equally ranked IID candidates
STEARYL ALCOHOLSTEARYL ALCOHOL2KR89I4H1YCREAM / TOPICAL162000 mgExact identifier — unii+route+dosage form
7 equally ranked IID candidates
.ALPHA.-TOCOPHEROL ACETATE.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0CAPSULE / ORAL2 mgExact identifier — unii candidate
21 equally ranked IID candidates
.ALPHA.-TOCOPHEROL ACETATE.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0FILM / BUCCAL0.09 mgExact identifier — unii candidate
21 equally ranked IID candidates
METHYLPARABENMETHYLPARABENA2I8C7HI9TCREAM / TOPICAL3000 mgExact identifier — unii+route+dosage form
7 equally ranked IID candidates
ASCORBIC ACIDASCORBIC ACIDPQ6CK8PD0RSOLUTION / TOPICAL0.04 %w/wExact identifier — unii+route
14 equally ranked IID candidates
LACTIC ACIDLACTIC ACID33X04XA5ATCREAM / TOPICAL1 %w/wExact identifier — unii+route+dosage form
7 equally ranked IID candidates

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 8 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Obagi Nu-Derm System Normal-Oily Skin TransformationHYDROQUINONE, TITANIUM DIOXIDE, ZINC OXIDEObagi Cosmeceuticals LLCef3ddd1e-9305-42bb-a5f8-559e8e641d832025-11-05WarningsExact identifier
ndc (package): 62032-100-36
ndc (package): 62032-101-36
ndc11 (package): 62032010136
ndc11 (package): 62032010036
Obagi Nu-Derm System Normal-Dry Skin TransformationHYDROQUINONE, TITANIUM DIOXIDE, AND ZINC OXIDEObagi Cosmeceuticals LLC750ea9a6-eedc-49db-8cef-1498ed41ad792025-11-04WarningsExact identifier
ndc (package): 62032-100-36
ndc (package): 62032-101-36
ndc11 (package): 62032010136
ndc11 (package): 62032010036
Obagi Nu-Derm System Normal-Dry Skin Transformation KitHYDROQUINONE, HOMOSALATE, OCTISALATE, ZINC OXIDEObagi Cosmeceuticals LLC16efa2db-8172-4026-a519-08f53d68b3c92025-10-23WarningsExact identifier
ndc (package): 62032-100-36
ndc (package): 62032-101-36
ndc11 (package): 62032010136
ndc11 (package): 62032010036
Obagi Nu-Derm System Normal-Oily Skin TransformationHYDROQUINONE, HOMOSALATE, OCTISALATE, ZINC OXIDEObagi Cosmeceuticals LLCe63327db-fb96-411c-945a-abe801d380452025-10-23WarningsExact identifier
ndc (package): 62032-100-36
ndc (package): 62032-101-36
ndc11 (package): 62032010136
ndc11 (package): 62032010036
Obagi Nu-Derm System Normal-Oily Skin Transformation TrialHYDROQUINONE, HOMOSALATE, OCTISALATE, ZINC OXIDEObagi Cosmeceuticals LLC219c68dc-1e74-4136-9065-85466008d4452025-10-23WarningsExact identifier
ndc (package): 62032-101-36
ndc11 (package): 62032010136
Obagi Nu-Derm System Normal-Dry Skin Transformation TrialHYDROQUINONE, HOMOSALATE, OCTISALATE, ZINC OXIDEObagi Cosmeceuticals LLCe2c23345-69df-47a1-8e6b-b6225080d3632025-10-23WarningsExact identifier
ndc (package): 62032-100-36
ndc (package): 62032-101-36
ndc11 (package): 62032010136
ndc11 (package): 62032010036
nu-derm system normal-dry skin transformationHYDROQUINONE, OCTISALATE AND ZINC OXIDEOBAGI COSMECEUTICAL LLC7548658a-5371-4aed-baf8-e5dc542622232025-03-14Warnings, Adverse reactionsExact identifier
ndc (package): 62032-100-36
ndc (package): 62032-101-36
ndc11 (package): 62032010136
ndc11 (package): 62032010036
NU-DERM BLENDER Skin Lightener and BlendingHYDROQUINONEObagi Cosmeceuticals LLCe5c450af-958e-41e3-9c2f-fda76b3596f52025-01-01Warnings, Adverse reactionsExact identifier
ndc (package): 62032-100-36
ndc (package): 62032-100-10
ndc (package): 62032-116-36
ndc (package): 62032-101-36
ndc (product): 62032-100
ndc (product): 62032-101
ndc (product): 62032-116
ndc11 (package): 62032010010
ndc11 (package): 62032010136
ndc11 (package): 62032010036
ndc11 (package): 62032011636
spl id: fbe3d3a3-ebf3-425c-9cd5-7b7d26054792
spl set id: e5c450af-958e-41e3-9c2f-fda76b3596f5

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.