Vivant True Tone

Manufacturer
Vivant Pharmaceuticals, LLC
Effective date
2025-07-24
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 20:35:34

Label at a glance#

ProductVivant True Tone
Active ingredientHYDROQUINONE
Label structure12 sections

Indications and uses

Uses ■ For the gradual fading of age spots ■ Lightens dark pigment in the skin ■This product provides minimal SPF protection.

Dosage and administration

Directions ■ Adult topical dosage is a thin layer to the affected area once or twicedaily■There is no recommended dosage for children under 12 years of age except under the advice and supervision of a doctor ■ Keep refrigerated

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Hydroquinone (2%)

Indication

OTC - PURPOSE SECTION

Skin Bleaching Agent

Uses

INDICATIONS & USAGE SECTION

Uses

■ For the gradual fading of age spots

■ Lightens dark pigment in the skin

■This product provides minimal SPF protection.

Warnings

WARNINGS SECTION

Warnings ■Sun exposure should be avoided indefinitely by using a high SPF sunscreen agent, a sunblocking agent, or protective clothing to cover bleached skin in order to prevent darkening from reoccurring ■ Do not get into eyes ■Keep out of reach of

children ■For external use only ■Not recommended for children under 12 years of age ■ If swallowed get medical help or contact a poison control center immediately.

Ask a doctor if you are:

OTC - ASK DOCTOR SECTION

using other topical acne medications

Directions

DOSAGE & ADMINISTRATION SECTION

Directions ■ Adult topical dosage is a thin layer to the affected area once or twicedaily■There is no recommended dosage for children under 12 years of age except under the advice and supervision of a doctor ■ Keep refrigerated

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Inactive Ingredients• Water, Mineral Oil, Propylene Glycol, Glyceryl Stearate, PEG-10O Stearate, Vitis Vinifera (Grape Seed) Seed Oil, Cetyl Alcohol, Emulsifying Wax, Caprylic/Capric Triglyceride, Retinyl Propionate, Kojic Acid, EthylhexylDimethyl PABA, Dimethicone, HydrolyzedOat Protein, Aloe Barbadensis Leaf Juice, Polyacrylamide, C13-14 isoparaffin, Laureth-7, Xanthan Gum, Sodium Hydroxide, Sodium Metabisulfite, Sodium Bisullte, Phenoxyethanol, Ethylhexylglycerin

When using this product

OTC - WHEN USING SECTION

if not improvement is seen after 2 months of treatment, use of this products should be discontinued

Stop use and ask the doctor if

OTC - STOP USE SECTION

excessive skin irritation develops or increases

Warnings

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children■For external only■Not recommended for children under12 years of age

Other Information

OTHER SAFETY INFORMATION

Other Information• Depigmentation(lightening) effect of this product may not be noticeable when used on very dark skin

This product will bleach skin and is not for the prevention of sunburn.

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
63750-00263750-002-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 24 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.

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Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
3ab1d20a-978f-4e79-e063-6394a90a317f10bc7194-0af6-3d77-e063-6394a90aea202025-07-24WarningsExact identifier
spl id: 3ab1d20a-978f-4e79-e063-6394a90a317f
spl set id: 10bc7194-0af6-3d77-e063-6394a90aea20

Reported adverse events (FAERS/openFDA)#

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