RUBELLI WATER GLOW SUN FOR GOLF

Manufacturer
RUBELLI CO.,LTD | WINNOVA Co., Ltd.
Effective date
2021-04-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:47:49

Label at a glance#

ProductRUBELLI WATER GLOW SUN FOR GOLF
Active ingredientOCTINOXATE, Homosalate, OCTISALATE, Titanium Dioxide
Label structure8 sections

Indications and uses

■ Helps prevent sunburn. ■ UV protection functional cosmetics with SPF50+, PA++++ which double-blocks ultraviolet UVA and UVB, and moisturizes the skin without tightness and has a refreshing feeling. BSASM™ which is seven plant complex patented ingredients are added, which calms down the skin tired by ultraviolet rays and makes the skin healthy.

Dosage and administration

■ Apply liberally and uniformly to all exposed areas 15-20 minutes before sun exposure. ■ Reapply often (every 2 hours) and after swimming, excessive perspiration and washing to ensure maximum sun protection.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

Ethylhexyl Methoxycinnamate 7.0%
Homosalate 3.0%
Ethylhexyl Salicylate 3.0%
Titanium Dioxide 1.66%

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Water, Butylene Glycol, Pentylene Glycol, Isononyl Isononanoate, Bis-Ethylhexyloxyphenol Methoxyphenyl Triazine, Niacinamide, Cocoglycerides, Ethylhexyl Triazone, Methyl Methacrylate Crosspolymer, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Polyglyceryl-10 Laurate, Caprylyl Glycol, Polyglyceryl-10 Myristate, Aluminum Hydroxide, Stearic Acid, Sodium Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Tocopheryl Acetate, Ethylhexylglycerin, Allantoin, Isohexadecane, Xanthan Gum, Sorbitan Isostearate, Adenosine, Polysorbate 80, 1,2-Hexanediol, Tulipa Gesneriana Flower Extract, Viola Mandshurica Flower Extract, Bellis Perennis (Daisy) Flower Extract, Citrus Aurantium Amara (Bitter Orange) Flower Extract, Iris Versicolor Extract, Glycerin, Sorbitan Oleate, Biosaccharide Gum-4
Centella Asiatica Extract, Scutellaria Baicalensis Root Extract, Polygonum Cuspidatum Root Extract, Aloe Barbadensis Leaf Extract, Glycyrrhiza Glabra (Licorice) Root Extract, Camellia Sinensis Leaf Extract, Chamomilla Recutita (Matricaria) Flower Extract, Rosmarinus Officinalis (Rosemary) Leaf Extract, Fragrance

PURPOSE

OTC - PURPOSE SECTION

Sunscreen

WARNINGS

WARNINGS SECTION

For external use only
- Do not use on damaged or broken skin
- When using this product, Keep out of eyes. Rinse with water to remove.
- Stop use and ask a doctor if rash occurs.
- Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If product is swallowed, get medical help or contact a Poison Control Center right away.

Uses

INDICATIONS & USAGE SECTION

■ Helps prevent sunburn.
■ UV protection functional cosmetics with SPF50+, PA++++ which double-blocks ultraviolet UVA and UVB, and moisturizes the skin without tightness and has a refreshing feeling. BSASM™ which is seven plant complex patented ingredients are added, which calms down the skin tired by ultraviolet rays and makes the skin healthy.

Directions

DOSAGE & ADMINISTRATION SECTION

■ Apply liberally and uniformly to all exposed areas 15-20 minutes before sun exposure.
■ Reapply often (every 2 hours) and after swimming, excessive perspiration and washing to ensure maximum sun protection.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71006-11071006-110-01, 71006-110-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
2f4d964f-cf71-4c1b-a29b-1f2a638ea38e49f521d2-5232-4511-aec5-d70454d9bbfe2021-06-04WarningsExact identifier
spl set id: 49f521d2-5232-4511-aec5-d70454d9bbfe

Reported adverse events (FAERS/openFDA)#

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