BAROX WHITE GOLF

Manufacturer
Barox Co., Ltd. | Gdkcosmetics Co., Ltd.
Effective date
2017-09-11
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 01:12:16

Label at a glance#

ProductBAROX WHITE GOLF
Active ingredientNiacinamide
Label structure8 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: Niacinamide 7.0%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Water, Butylene Glycol, Mineral Oil, Petrolatum, Cetyl Ethylhexanoate, Glycerin, Glyceryl Stearate, Cetearyl Alcohol, Arbutin, Caprylic/Capric Triglyceride, Cetearyl Alcohol, Beeswax, Macadamia Ternifolia Seed Oil, Stearic Acid, Dimethicone, Sorbitan Sesquioleate, PEG-100 Stearate, PEG-40 Stearate, PEG-20 Stearate, Triethanolamine, Phenoxyethanol, Carbomer, Methylparaben, Fragrance, Silk Amino Acids, Tocopheryl Acetate, Propylparaben, Disodium EDTA, Dimethyl Sulfone, Sodium Hyaluronate, Ethylhexylglycerin, Avena Strigosa Seed Extract, Morinda Citrifolia Extract, Lavandula Angustifolia (Lavender) Extract, Melissa Officinalis Extract, Oryza Sativa (Rice) Extract, Aloe Barbadensis Leaf Juice, Usnea Barbata (Lichen) Extract, Zanthoxylum Piperitum Fruit Extract

PURPOSE

OTC - PURPOSE SECTION

Purpose: Skin Protectant (Brightening)

WARNINGS

WARNINGS SECTION

Warning: 1. In case of having following symptoms after using this, you're advised to stop using it immediately. If you keep using it, the symptoms will get worse and need to consult a dermatologist. 1) In case of having problems such as red rash, swollenness, itching, stimulation during usage. 2) In case of having the same symptoms above on the part you put this product on by direct sunlight. 2. You are banned to use it on the part where you have a scar, eczema, or dermatitis. 3. In case of getting it into your eyes, you have to wash it immediately.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children: Keep out of reach of babies and children

INDICATIONS & USAGE

INDICATIONS & USAGE SECTION

Indications & Usage: Pump 1-2 times and spread following the skin texture, tap lightly for better absorption

DOSAGE & ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

Dosage & Administration: Take an adequate amount of this product.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

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
55692-01055692-010-01

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
Niacinamide25X51I8RD4ACTIB
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
314eaa2f-4f12-4ea6-af65-bc34babaabe4a82a5204-c4bf-42bf-9121-68b363fee41b2019-11-07WarningsExact identifier
spl set id: a82a5204-c4bf-42bf-9121-68b363fee41b

Reported adverse events (FAERS/openFDA)#

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