Body Fade Creme

Manufacturer: Biocosmetic Reasearch Labs
Effective date: 2009-12-08
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: full-release
Hydrated at: 2026-05-31 22:25:17

Label at a glance#

ProductBody Fade Creme Maximum Strength

Active ingredientHydroquinone

Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient

Hydroquinone 2%

OTC - PURPOSE SECTION

Purpose

Skin Lightener Cream

INDICATIONS & USAGE SECTION

Uses

For gradual fading of dark (brownish) spots.

WARNINGS SECTION

Warnings

Avoid contact with eyes.

OTC - DO NOT USE SECTION

Do not use on children under 12 years of age.

OTC - STOP USE SECTION

Some users may experience a mild irritation. If skin Irritation becomes severe, stop use and consult a doctor.

DOSAGE & ADMINISTRATION SECTION

Directions

Apply all over your body twice daily. Pay special attention to problem areas like knees and elbows.

INACTIVE INGREDIENT SECTION

Inactive Ingredients

Water (Aqua), Isopropyl Palmitate, Stearic Acid, Propylene Glycol, Cetyl Alcohol, DEA-Cetyl Phosphate, glycerin, Dimethicone, Tocopheryl Acetate, Sodium PCA, Aloe Barbadensis Leaf Extract, Citrus Unshiu Peel Extract, Sodium Palmitoyl Proline, Nymphaea Alba Flower Extract, Polyacrylamide, Hydroxyethylcellulose, Fragrance, C13-14 Isoparaffin, Laureth-7, EDTA, Sodium Sulfite, Sodium Metabisulfite, Diazolidinyl Urea, Iodopropynyl Butylcarbamate, Blue 1 (CI 42090), Yellow 5 (CI 19140)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of Carton

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
153031	hydroquinone 2 % Topical Cream	PSN	3
153031	hydroquinone 20 MG/ML Topical Cream	SCD	3
153031	hydroquinone 2 % Topical Cream	SY	3

DailyMed Pharmacologic Classes#

Class, Version, Type table
Class	Version	Type	Effective
HYDROQUINONE Pharmacologic Class Indexing	2	Indexing - Pharmacologic Class	20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
85490a6b-2306-6bf2-c51b-eb63537dc2da	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
59735-304-63	2020-01-31	C162847	48780-1	9d75b9d1-0093-f424-e053-dadaa90a57ce	Body Fade Creme Maximum Strength

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
59735-304-63	Body Fade CremeMaximum Strength	1 in 1 CARTON	CREAM	1		3
59735-304-63	Body Fade CremeMaximum Strength	180 g in 1 TUBE	CREAM	180		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
59735-304	BODY FADE CREME MAXIMUM STRENGTH (HYDROQUINONE ) CREAM [BIOCOSMETIC REASEARCH LABS]	3	Legacy NDC, 2 package rows	20100722_42438712-30c6-4e33-bb6e-a29b5e005b23.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version	Uploaded
Hydroquinone	ACTIVE INGREDIENT	XV74C1N1AE	3
Hydroquinone	ACTIVE MOIETY	XV74C1N1AE	3

Products#

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

DailyMed product names page 1 of 1 · 2 matching rows.

Body Fade Creme Maximum Strength
Hydroquinone

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
59735-304	59735-304-63

Ingredients#

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

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

Name, UNII, Kind table
Name	UNII	Kind
Hydroquinone	XV74C1N1AE	ACTIB

Source Document#

Source XML

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 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
61be7ea1-7188-4fd6-9c3a-81b0eb76fff4			42438712-30c6-4e33-bb6e-a29b5e005b23	2009-12-08	Warnings	Exact identifier spl id: 61be7ea1-7188-4fd6-9c3a-81b0eb76fff4 spl set id: 42438712-30c6-4e33-bb6e-a29b5e005b23

Reported adverse events (FAERS/openFDA)#

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