Dolly Intense Lightening

Manufacturer
Mitchell Cosmetics, Inc. | Cabinet Continental
Effective date
2020-08-27
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:16:53

Label at a glance#

ProductDolly Intense Lightening
Active ingredientHYDROQUINONE
Label structure17 sections

Indications and uses

Lightening Treatment and skin lightener

Dosage and administration

Apply a thin layer of lotion preferably at night to clean dry skin

Storage and handling

Store in cool dry place

Label contents#

Full prescribing information#

DOLLY INTENSE LIGHTENING LOTION STATEMENT OF IDENTITY

STATEMENT OF IDENTITY SECTION

Intense LIghtening Lotion

DOLLY INTENSE LIGHTENING LOTION DOSAGE AND ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

Apply a thin layer of lotion preferably at night to clean dry skin

DOLLY INTENSE LIGHTENING LOTION ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Hydroquinone 2%

DOLLY INTENSE LIGHTENING LOTION

OTC - ASK DOCTOR SECTION

If in doubt, consult with your physiciian. Stop use and ask a doctor if skin rash occurs.

DOLLY INTENSE LIGHTENING LOTION

OTC - DO NOT USE SECTION

IF pregnant or nursing do not use product containing hydroquinone.

DOLLY INTENSE LIGHTENING LOTION KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help

DOLLY INTENSE LIGHTENING LOTION PREGNANCY OR BREAST FEEDING SECTION

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or nursing do not use product containing hydroquinone. Discpntinue the use of skin care products containing hydroquinone for at least one month before contemplating pregnanacy. If in doubt, consult with your physician.

DOLLY INTENSE LIGHTENING LOTION PURPOSE

OTC - PURPOSE SECTION

Lightening Treatmenet Lotion Skin Lightener

DOLLY INTENSE LIGHTENING LOTION STOP USE

OTC - STOP USE SECTION

Stop use and ask a doctor is skin rash occurs

DOLLY INTENSE LIGHTENING LOTION DESCRIPTION

DESCRIPTION SECTION

Nourishes and moistures skin while working to even out skin tone, improviding clarity and radiance. Promotes softer and smoother skin.

DOLLY INTENSE LIGHTENING LOTION

WARNINGS SECTION

For external use only

DOLLY INTENSE LIGHTENING LOTION ENVIRONMENTAL WARNING

ENVIRONMENTAL WARNING SECTION

This product is not for use in the prevent of sunburn. To avoid further pigmentation, always follow up with an SPF 30 or higher during and after brightening treatment.

DOLLY INTENSE LIGHTENING LOTION GENERAL PRECAUTIONS

GENERAL PRECAUTIONS SECTION

Avoid contact with eyes. Rinse with water to remove

DOLLY INTENSE LIGHTENING LOTION STORAGE AND HANDLING

STORAGE AND HANDLING SECTION

Store in cool dry place

DOLLY INTENSE LIGHTENING LOTION INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

water, slyceryl stearate, IPM, glycerin, cetearyl alcohol, p-chloro-m-cresol, fragrance, tocopheryl acetate, allantoin, ascorbic acid, sodium lauryl sulfate, sodium metabisulfite, disodium EDTA, methylparaben, propylparaben, OMC, Sodium Sulfite, Sodium Chloride, Clove Oil, Cithrol DPHS-So-TH, Down Corning 5200

DOLLY INTENSE LIGHTENING LOTION INDICATIONS AND USAGE

INDICATIONS & USAGE SECTION

Lightening Treatment and skin lightener

DOLLY INTENSE LIGHTENING LOTION PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Dolly Intense Lightening LotionDolly Intense Lightening Lotion

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79009-10579009-105-25

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
HYDROQUINONEXV74C1N1AEACTIB
WATER059QF0KO0RIACT

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
d4619054-0702-1fea-e053-2a95a90a39dcaddf8707-dc3d-9752-e053-2995a90a8fa82021-12-30WarningsExact identifier
spl set id: addf8707-dc3d-9752-e053-2995a90a8fa8

Reported adverse events (FAERS/openFDA)#

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