Corrector 2 Hydroquinone Cream

Manufacturer
Vivier Pharma Inc. | Entreprises ImportFAB Inc.
Effective date
2021-01-07
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
legacy-cache
Hydrated at
2026-08-01 22:57:46

Label at a glance#

ProductCORRECTOR 2
Active ingredientHYDROQUINONE
Label structure8 sections

Dosage and administration

Use fingertips to apply a thin layer to affected areas. Use both morning and night or as directed by a physician. Close cap securely after each use.

Label contents#

Full prescribing information#

MEDICINAL INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

2.0% Hydroquinone USP

PURPOSE

OTC - PURPOSE SECTION

Skin Bleaching and Correcting

USE

INDICATIONS & USAGE SECTION

  • To gradually lighten hyperpigmentation of the skin such as age spots, liver spots, freckles or hyperpigmentation that can occur as a result of pregnancy or from the use of oral contraceptives.

WARNINGS

WARNINGS SECTION

For external use only.Use only on the advice of a physician.

Do not use

OTC - DO NOT USE SECTION

  • On broken or irritated skin.
  • On children under 12 years of age.
  • If you are pregnant or nursing unless instructed by a physician.

Allergy alert:

SPL UNCLASSIFIED SECTION

Contains Sodium Metabisulfite.

Sunburn alert:

SPL UNCLASSIFIED SECTION

Limit sun exposure during treatment by using protective clothing or a sunscreen protective agent to avoid re-darkening of the skin.

When using this product

OTC - WHEN USING SECTION

  • A mild transient stinging may occur for people with sensitive skin.
  • Gradual lightening of the discolored area can be expected in most cases.
  • Avoid contact with eyes and mucous membranes.  In case of contact, rinse thoroughly with water.

Stop using this product

OTC - STOP USE SECTION

  • If irritation or rash occurs.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

  • Use fingertips to apply a thin layer to affected areas.
  • Use both morning and night or as directed by a physician.
  • Close cap securely after each use.

NON-MEDICINAL INGREDIENTS

INACTIVE INGREDIENT SECTION

Butylated Hydroxy Toluene, Butylparaben, Cetearyl Alcohol, Cetyl Alcohol, Disodium EDTA, Ethoxydiglycol, Fragrance, Glycerin, Lactic Acid, L-Ascorbic Acid USP, Methylparaben, Phenyl Trimethicone, PPG-2 Myristyl Ether Propionate, Propylparaben, Sodium Cetearyl Sulfate, Sodium Lauryl Sulfate, Sodium Metabisulfite, Tocopheryl Acetate, Water/Eau.

Questions?

OTC - QUESTIONS SECTION

​450 455 9779              1 877 484 8437

SPL UNCLASSIFIED SECTION

Store at room temperature (15-30 ​o​C / 59-86 ​o​F).  See package insert for complete details.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1133

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
67226-282267226-2822-6

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
d9b5473e-a5e3-3a3b-e053-2a95a90a5d73edbde739-70ef-4bb5-b109-6afead84c5ed2022-03-08WarningsExact identifier
spl set id: edbde739-70ef-4bb5-b109-6afead84c5ed

Reported adverse events (FAERS/openFDA)#

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