Olivia Quido Skincare Blemish Eraser

Manufacturer
O Skin Care LLC | V Manufacturing & Logistics, Inc.
Effective date
2021-07-27
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:39:34

Label at a glance#

ProductOlivia Quido Skincare Blemish Eraser
Active ingredientHYDROQUINONE
Label structure9 sections

Indications and uses

For the gradual fading of dark blemishes in the skin such as age spots, freckles, liver spots.

Dosage and administration

Adults: apply a small amount as a thin layer on the affected area twice daily, or use as directed by a physician. If no improvement is seen after 3 months of treatment, use of this product should be discontinued. Lightening effect of this product may not be noticeable when used on dark skin. Children under 12 years old: do not use unless directed by a physician. Sun exposure should be limited by using a sunscreen ...

Storage and handling

Store at a controlled room temperature: 15°-30°C (59°-86°F), away from direct sunlight.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Hydroquinone, 2%

Purpose

OTC - PURPOSE SECTION

Skin Lightening

Uses

INDICATIONS & USAGE SECTION

For the gradual fading of dark blemishes in the skin such as age spots, freckles, liver spots.

Warnings

WARNINGS SECTION

For external use only.

Do Not Use on Children - under 12 years old of age unless directed by a physician.

OTC - DO NOT USE SECTION

Do not use on children - under 12 years of age unless directed by a physician.

OTC - STOP USE SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of eyes. Rinse water to remove.

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • Adults: apply a small amount as a thin layer on the affected area twice daily, or use as directed by a physician.
  • If no improvement is seen after 3 months of treatment, use of this product should be discontinued.
  • Lightening effect of this product may not be noticeable when used on dark skin.
  • Children under 12 years old: do not use unless directed by a physician.
  • 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.

Other Information

STORAGE AND HANDLING SECTION

  • Store at a controlled room temperature: 15°-30°C (59°-86°F), away from direct sunlight.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

4-Butylresorcinol, Aloe Barbadensis Leaf Juice, BHT, C13-14 Isoparaffin, Caprylic/Capric Triglyceride, Carthamus Tinctorius (Safflower) Oleosomes, Ceramide - NP, Cetyl Palmitate, Cetyl PEG/PPG-10/1 Dimethicone, Citric Acid, Diazolidinyl Urea, Dimethyl Isosorbide, Glycerin, Hexyl Laurate, Iodopropnyl Butylcarbamate, Kojic Acid, Laureth-23, Laureth-7, Maltodextrin, Phenoxyethanol, Polyacrylamide, Polyglyceryl-4 Isostearate, Polysorbate 20, Retinol, Silica, Sodium Hyaluronate, Sodium Hydroxide, Tetrahexyldecyl Ascorbate, Tocopheryl Acetate, Trideceth-6 Phosphate, Triethylene Glycol, Water/Aqua.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

OSCBEOSCBE

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71421-501-302024-08-21C16284748780-1e4f33bdf-ae3a-d8a0-e053-dadaa90a6e4eOlivia Quido Skincare Blemish Eraser
71421-501-302022-07-29C16284748780-1e4f33bdf-ae3a-d8a0-e053-dadaa90a6e4eOlivia Quido Skincare Blemish Eraser

Products#

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

DailyMed product names page 1 of 1 · 31 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71421-50171421-501-30

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 30 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
2035bfab-4915-0e91-e063-6294a90a7b22c8265b99-3df9-42c6-e053-2995a90a2a2d2024-08-21WarningsExact identifier
spl set id: c8265b99-3df9-42c6-e053-2995a90a2a2d

Reported adverse events (FAERS/openFDA)#

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