Bling Magic Speedy Brightening Moisturizer

Manufacturer
GRU INTERNATIONAL
Effective date
2016-05-09
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:45:54

Label at a glance#

ProductBling Magic Speedy Brightening Moisturizer
Active ingredientDimethicone
Label structure8 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: Dimethicone 1.0%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Water, Butylene Glycol, Cyclomethicone, Polyglutamic Acid, Arbutin, Glycerin, Titanium Dioxide, Dimethicone/Vinyl Dimethicone Crosspolymer, Cetyl PEG/PPG-10/1 Dimethicone, Sodium Chloride, Aluminum Hydroxide, Triethoxycaprylylsilane, Adenosine, Lavandula Angustifolia (Lavender) Flower Extract, Monarda Didyma Leaf Extract, Mentha Piperita (Peppermint) Leaf Extract, Freesia Alba Flower Extract, Chamomilla Recutita (Matricaria) Flower/Leaf Extract, Rosmarinus Officinalis (Rosemary) Leaf Extract, Glycyrrhiza Glabra (Licorice) Root Extract, Diospyros Kaki Leaf Extract, Morus Alba Bark Extract, Opuntia Ficus-Indica Extract, Zanthoxylum Piperitum Fruit Extract, Pulsatilla Koreana Extract, Aloe Barbadensis Leaf Extract, Cirsium (Thistle) Flower/Leaf/Stem Extract, Usnea Barbata (Lichen) Extract, 1,2-Hexanediol, Caprylyl Glycol, Fragrance

PURPOSE

OTC - PURPOSE SECTION

Purpose: Skin Protectant

WARNINGS

WARNINGS SECTION

Warnings: 1. If the following side effects occur, immediately discontinue use. Before resuming use, consult a dermatologist as continual use may worsen symptoms. A) If red spots, swelling, itching, irritation, or other discomforts occur after using the product. B) If the above symptoms occur on the applied area after exposure to direct sunlight. 2. Do not use on open wounds or on areas of skin exhibiting signs of eczema or dermatitis. 3. Storage and handling precautions A) Keep product out of reach of infants and children. B) Ensure that lid is closed after use. C) Do not store in places subject to high or cold temperatures or under exposure to direct sunlight. D) Use care to avoid eye contact when using this product.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep product out of reach of infants and children.

INDICATIONS & USAGE

INDICATIONS & USAGE SECTION

Indications & usage: Take some of the essence on your palm and rub it on your face and neck. You will stage a much brighter and beautiful skin. If you wish to stage your skin tone even brighter, simply apply more. It can also be used on the back of your hands, elbows and knees to stage brighter skin.

DOSAGE & ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

Dosage & Administration: Take an adequate amount of this product depending on the brightness of skin you would like to stage.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
DIMETHICONE Pharmacologic Class Indexing3Indexing - Pharmacologic Class20180813

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70653-010-022020-01-31C16284748780-19d75b9d0-fbc5-f424-e053-dadaa90a57ce4fb4cfeb-a528-452f-8b29-5731214d5076

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70653-010-01Bling Magic Speedy Brightening Moisturizer15 mL in 1 TUBECREAM152
70653-010-02Bling Magic Speedy Brightening Moisturizer1 in 1 CARTONCREAM12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70653-010BLING MAGIC SPEEDY BRIGHTENING MOISTURIZER (DIMETHICONE) CREAM [GRU INTERNATIONAL]2Legacy NDC, 2 package rows20160509_4fb4cfeb-a528-452f-8b29-5731214d5076.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70653-01070653-010-01, 70653-010-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
Dimethicone92RU3N3Y1OACTIB
Water059QF0KO0RIACT
Butylene Glycol3XUS85K0RAIACT

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
fcde9f23-1b38-4db4-a53c-f868cbf8f7ff4fb4cfeb-a528-452f-8b29-5731214d50762016-05-09WarningsExact identifier
spl id: fcde9f23-1b38-4db4-a53c-f868cbf8f7ff
spl set id: 4fb4cfeb-a528-452f-8b29-5731214d5076

Reported adverse events (FAERS/openFDA)#

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