BANILA CO Prime Primer Sun

Manufacturer
F&CO Co., Ltd. | Cosmax, Inc
Effective date
2017-11-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:10:24

Label at a glance#

ProductBANILA CO Prime Primer Sun
Active ingredientAvobenzone, Octinoxate, Octocrylene, Octisalate, Homosalate, Ensulizole
Label structure6 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENTS: Butyl Methoxydibenzoylmethane 3.5%, Ethylhexyl Methoxycinnamate 6.9%, Octocrylene 2.0%, Ethylhexyl Salicylate 4.5%, Homosalate 3.0%, Phenylbenzimidazole Sulfonic Acid3.5%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENTS: Water, Butylene Glycol, Ethylhexyl Palmitate, Niacinamide, Pentaerythrityl Distearate, Bis-Ethylhexyloxyphenol Methoxyphenyl Triazine, Caprylic/Capric Triglyceride, Aminomethyl Propanol, Sodium Polyacrylate, C12-15 Alkyl Benzoate, Ethylhexyl Stearate, Glyceryl Stearate, Methyl Methacrylate Crosspolymer, PEG-100 Stearate, Sodium Stearoyl Glutamate, Polysorbate 60, Dipropylene Glycol Dibenzoate, Phenoxyethanol, Caprylyl Glycol, Fragrance(Parfum), Glyceryl Caprylate, PPG-15 Stearyl Ether Benzoate, Trideceth-6, Adenosine, Xanthan Gum, Disodium EDTA, Jasminum Officinale (Jasmine) Flower/Leaf Extract, Nelumbo Nucifera Flower Extract, Freesia Refracta Extract, Iris Versicolor Extract, Leontopodium Alpinum Flower/Leaf Extract, Lilium Candidum Bulb Extract, Narcissus Pseudo-Narcissus (Daffodil) Flower Extract, Rose Extract

PURPOSE

OTC - PURPOSE SECTION

PURPOSE: Sunscreen

WARNINGS

WARNINGS SECTION

WARNINGS: If redness or irritation occurs, discontinue use, and consult a dermatologist. Do not use on broken skin. For external use only. Replace the cap after use. Keep out of reach of children. Do not expose to heat or direct sunlight. Do not store at high temperatures. Avoid contact with eyes.

INDICATION AND USAGE

DESCRIPTION SECTION

INDICATION AND USAGE: Evenly spread moderate amount on skin on final skin care.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69106-43069106-430-01, 69106-430-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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
ef3cafa2-5e11-402f-9b58-0bb80e2cf67229a56f83-e179-4d25-927e-63d50ae542c72017-11-08WarningsExact identifier
spl id: ef3cafa2-5e11-402f-9b58-0bb80e2cf672
spl set id: 29a56f83-e179-4d25-927e-63d50ae542c7

Reported adverse events (FAERS/openFDA)#

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