Body Merry Lightening and Whitening Cream

Manufacturer
Body Merry, LLC
Effective date
2021-01-15
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:56:07

Label at a glance#

ProductBody Merry Lightening and Whitening Cream
Active ingredientHYDROQUINONE
Label structure8 sections

Indications and uses

For gradual fading of hyperpigmented areas of the skin. Helps fade away dark spots on the skin.

Dosage and administration

Apply onto cleansed skin of the affected area or as directed by a physician. Not recommended for children under 12 years of age.

Label contents#

Full prescribing information#

Active Ingredients/Purpose:

OTC - ACTIVE INGREDIENT SECTION

Hydroquinone 2.0% Skin Lightener

Active Ingredient/Purpose:

OTC - PURPOSE SECTION

Skin Lightener

Warnings:

WARNINGS SECTION

For external use only. Do not use on inflammed or broken skin. When using this product, avoid contact with the eyes. If contact occurs, rinse thoroughly with water. Avoid unnecessary sun exposure and use a sunscreen or protective clothing. Stop use and consult a doctor if irritation becomes severe. If pregnant or breastfeeding, consult a physician before use. Keep out of reach of children.

Uses

INDICATIONS & USAGE SECTION

For gradual fading of hyperpigmented areas of the skin. Helps fade away dark spots on the skin.

Directions:

DOSAGE & ADMINISTRATION SECTION

Apply onto cleansed skin of the affected area or as directed by a physician. Not recommended for children under 12 years of age.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

water, glyceryl streate, PEG-100 stearate, stearic acid

Warning

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Body Merry Lightening and Whitening Cream CopyBody Merry Lightening and Whitening Cream Copy

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73428-100173428-1001-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
dda47916-24d5-fbec-e053-2a95a90abee59753e922-15dc-3dd2-e053-2a95a90a62bd2022-04-27WarningsExact identifier
spl set id: 9753e922-15dc-3dd2-e053-2a95a90a62bd

Reported adverse events (FAERS/openFDA)#

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