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OTC

Note BB 500

octinoxate · Note BB 500 is an over-the-counter drug containing octinoxate, made by ALTONA COSMETICS TECHNOLOGY SANAYI VE TICARET ANONIM SIRKETI.

Type
Over the counter
Drug class
Not classified
Route
Topical
Manufacturers
1

helps prevent sunburn if used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun

Drug facts

Generic name
octinoxate
Active ingredients
Octinoxate
Dosage forms
Cream
Label holder
ALTONA COSMETICS TECHNOLOGY SANAYI VE TICARET ANONIM SIRKETI
FDA application
M020
Label updated
09/16/2024

Active ingredients

Octinoxate 0.6% Purpose Sunscreen

Purpose

Sunscreen

Uses

Helps prevent sunburn if used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun

Directions

Apply liberally 15 minutes before sun exposure Reapply at least every 2 hours Use a water resistant sunscreen if swimming or sweating Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including: limit time in the sun, especially from 10 a.m.-2 p.m. wear long-sleeved shirts, pants, hats, and sunglasses Children under 6 months of age: Ask a doctor

Warnings

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

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

Rash occurs.

Keep out of reach of children

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

Inactive ingredients

Water (Aqua), Cyclopentasiloxane, PEG-10 Dimethicone, Butylene Glycol, Dimethicone, HDI/Trimethylol Hexyllactone Crosspolymer, Mica, Disteardimonium Hectorite, Aluminum Starch Octenylsuccinate, Phenoxyethanol, Alcohol, Glycerin, Tocopheryl Acetate, Trimethylsiloxysilicate, Bran (Triticum vulgare) Extract, Dimethicone/Vinyl Dimethicone Crosspolymer, Sodium Chloride, Triethoxycaprylylsilane, Propylene Glycol, Ethylhexylglycerin, Fragrance (Parfum), Silica, BHT, Bitter Orange(Citrus aurantium) Fruit Extract, Grapefruit (Citrus paradisi) Fruit Extract, Lecithin, Sorbitol, Sodium Ascorbate, Sunflower (Helianthus annus) Seed Oil, Tocopherol, Sodium Hydroxide. May contain: Titanium Dioxide (CI 77891), Iron Oxides (CI 77491, CI 77492, CI 77499)

Forms and strengths

From the FDA NDC Directory · 1 product codes

Dosage formStrengthRouteNDCs
Cream6 mg/mLtopical1

Manufacturers and labels

1 FDA label

  • ALTONA COSMETICS TECHNOLOGY SANAYI VE TICARET ANONIM SIRKETIShown hereM020 · Label 09/16/2024 · NDC 70474-024Full label

Related recalls

FDA drug recalls that name this drug or its active ingredient

All drug recalls

Note BB 500: common questions

What is Note BB 500 used for?
helps prevent sunburn if used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun
Is Note BB 500 a prescription drug?
No. Note BB 500 is sold over the counter (OTC) without a prescription.
Are there other products with the same active ingredient as Note BB 500?
Yes. Other FDA-listed products with the same active ingredients include Giorgio Armani Power Fabric Plus Weightless Matte Foundation Broad Spectrum SPF 25 Sunscreen, Lancome Paris Renergie Lift Makeup Broad Spectrum SPF 26 Sunscreen, Lancome Paris Skin Feels Good Broad Spectrum SPF 23 Sunscreen Hydrating Skin Tint Healthy Glow, Covergirl Outlast Extreme Wear 3-in-1 Foundation 24 HR Full Coverage SPF 18 Octinoxate Sunscreen Liquid Foundation.
Who makes Note BB 500?
ALTONA COSMETICS TECHNOLOGY SANAYI VE TICARET ANONIM SIRKETI lists Note BB 500 with the FDA.

Source: U.S. Food and Drug Administration, openFDA drug label (SPL) and NDC Directory · Last updated 09/16/2024 · Label text is shown as published by the manufacturer. Not medical advice