BANILA CO Prime Primer Fitting BB Natural Beige

Manufacturer
F&CO Co., Ltd. | Cosmax, Inc
Effective date
2017-11-07
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:10:34

Label at a glance#

ProductBANILA CO Prime Primer Fitting BB Natural Beige
Active ingredientTitanium Dioxide, Zinc Oxide, Octinoxate
Label structure6 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENTS: Titanium Dioxide 9.69%, Zinc Oxide 2.94%, Ethylhexyl Methoxycinnamate 5.0%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENTS: Cyclopentasiloxane, Water, C30-45 Alkyl Cetearyl Dimethicone Crosspolymer, Dimethicone, PEG-10 Dimethicone, Pentylene Glycol, Triethylhexanoin, Methyl Methacrylate Crosspolymer, Dimethicone/Vinyl Dimethicone Crosspolymer, Disteardimonium Hectorite, Sodium Chloride, Iron Oxides (CI 77492), Phenoxyethanol, Sorbitan Sesquioleate, Aluminum Hydroxide, Glyceryl Behenate, Polyglyceryl-6 Octastearate, Iron Oxides (CI 77491), Stearic Acid, Fragrance(Parfum), Triethoxycaprylylsilane, Iron Oxides (CI 77499), Ethylhexylglycerin, Disodium EDTA, Silica, Butylene Glycol, Fomes Officinalis (Mushroom) Extract, Glycerin, Phenyl Trimethicone, Carrageenan, Portulaca Oleracea Extract, PEG-40 Hydrogenated Castor Oil, Hydrogenated Lecithin, Propylene Glycol, Algin, Chlorphenesin, Potassium Sorbate, Sodium Benzoate, Sodium Dehydroacetate, Citric Acid, Sorbic Acid, Polysorbate 60

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.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69106-42069106-420-01, 69106-420-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Source Document#

Source XML

openFDA label cross-check#

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Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
18d17600-2cf8-448c-95cc-ae54d17975f9b1c7e68f-b99d-4dc0-9fe0-74efd02608a22020-01-03WarningsExact identifier
spl set id: b1c7e68f-b99d-4dc0-9fe0-74efd02608a2

Reported adverse events (FAERS/openFDA)#

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