MULTI COMPLEX FADE

Manufacturer: CONTROL CORRECTIVE SKINCARE INC
Effective date: 2018-11-11
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: legacy-cache
Hydrated at: 2026-08-02 00:47:15

Label at a glance#

ProductMULTI COMPLEX FADE

Active ingredientHYDROQUINONE

Label structure9 sections

Dosage and administration

APPLY A SMALL AMOUNT TO AFFECTED AREA ONCE OR TWICE DAILY. TO AVOID IRRITATION, BEGIN GRADUALLY. AVOID USING PRODUCTS THAT CONTAIN PEROXIDE AT THE SAME TIME. DAILY USE OF SUNSCREEN IS REQUIRED.

Contacts and useful links#

PhoneLabel contact1-866-290-4290

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

HYDROQUINONE (2%)

PURPOSE

OTC - PURPOSE SECTION

SKIN LIGHTENER

USE

INDICATIONS & USAGE SECTION

FOR THE GRADUAL FADING OF HYPERPIGMENTATION SPOTS.

WARNINGS

WARNINGS SECTION

FOR EXTERNAL USE ONLY. AVOID CONTACT WITH EYES. SOME USERS OF THIS PRODUCT MAY EXPERIENCE A MILD SKIN IRRITATION, IF SKIN IRRITATION BECOMES SEVERE, STOP USE AND CONSULT A DOCTOR.

DO NOT USE ON CHILDREN UNDER 12 YEARS OF AGE UNLESS DIRECTED BY A DOCTOR.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN. IF SWALLOWED, GET MEDICAL ATTENTION OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

APPLY A SMALL AMOUNT TO AFFECTED AREA ONCE OR TWICE DAILY.
TO AVOID IRRITATION, BEGIN GRADUALLY.
AVOID USING PRODUCTS THAT CONTAIN PEROXIDE AT THE SAME TIME.
DAILY USE OF SUNSCREEN IS REQUIRED.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

WATER, GLYCOLIC ACID, KOJIC ACID, HYDROXYETHYLCELLULOSE, GLYCYRRHIZA GLABRA (LICORICE) ROOT EXTRACT, SALIX ALBA (WILLOW) BARK EXTRACT, IMIDAZOLIDINYL UREA.

QUESTIONS?

OTC - QUESTIONS SECTION

1-866-290-4290

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

01b UC_Multi Complex Fade Gel

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

MULTI COMPLEX FADE
HYDROQUINONE
WATER
GLYCOLIC ACID
KOJIC ACID
HYDROXYMETHYL CELLULOSE
LICORICE
WILLOW BARK
IMIDUREA

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
70764-301	70764-301-11, 70764-301-51

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
HYDROQUINONE	XV74C1N1AE	ACTIB
WATER	059QF0KO0R	IACT
GLYCOLIC ACID	0WT12SX38S	IACT
KOJIC ACID	6K23F1TT52	IACT
HYDROXYMETHYL CELLULOSE	273FM27VK1	IACT
LICORICE	61ZBX54883	IACT
WILLOW BARK	S883J9JDYX	IACT
IMIDUREA	M629807ATL	IACT

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
05f609b5-8d09-9b7b-e063-6394a90ad8ba			07ca79f3-a199-4e53-b85e-cdc833276075	2023-09-22	Warnings	Exact identifier spl set id: 07ca79f3-a199-4e53-b85e-cdc833276075

Reported adverse events (FAERS/openFDA)#

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