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Over-the-counter medicine · no prescription needed

Avobenzone, octinoxate, octisalate, octocrylene, oxybenzone and titanium dioxide

Purpose on the label: Sunscreen

Sunscreens

Official FDA data, not advice

The label text is quoted exactly as the company filed it with the U.S. Food and Drug Administration (FDA), with a link to the official copy. The list of brands comes from the FDA NDC Directory.

This page is not medical advice. Read the label on your package, and ask a pharmacist or doctor if you are not sure a medicine is right for you, for your child, or with your other medicines.

If someone may have taken too much, call Poison Help: 1‑800‑222‑1222. In an emergency, call 911.

Quick answers

What is Avobenzone, octinoxate, octisalate, octocrylene, oxybenzone and titanium dioxide used for?
The Drug Facts label of Brush and Go All Skin types (Noon Aesthetics M.R. Ltd) lists these uses: help prevent sunburn.
Do I need a prescription for Avobenzone, octinoxate, octisalate, octocrylene, oxybenzone and titanium dioxide?
No. The products on this page are sold without a prescription (over the counter).
Is a store brand the same as the name brand?
Products listed together below have the same active ingredients, in the same amount and the same form, as registered with the FDA. Inactive ingredients (such as colors, flavors and fillers) and package sizes can differ. Compare the “Active ingredient” box on both packages, and ask a pharmacist if you are not sure.
Has Avobenzone, octinoxate, octisalate, octocrylene, oxybenzone and titanium dioxide been recalled?
No recall linked to these products appears in the FDA enforcement reports we use.

Drug Facts label

Every over-the-counter medicine must carry a “Drug Facts” box in the same order, set by FDA rules. Below is the label of one product for each common strength and form, quoted word for word. Your own package can differ (for example, children’s products have other directions): always follow the label on your package.

Brush and Go All Skin types · Noon Aesthetics M.R. Ltd

Avobenzone 0.075 g/5 g · Octinoxate 0.236 g/5 g · Octisalate 0.135 g/5 g · Octocrylene 0.225 g/5 g · Oxybenzone 0.075 g/5 g · Titanium dioxide 1.25 g/5 g, powder (topical)

Active ingredient

Titanium Dioxide 25% Ethylhexyl Methoxycinnamate 4.7% Octocrylene 4.5% Ethylhexyl Salicylate 2.7% Butyl Methoxydibenzoylmethane 1.5% Benzophenone 1.5% Purpose Sunscreen

Purpose

Sunscreen

Uses

help prevent sunburn

Warnings

For external use only

Do not use

on damage 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.

Directions

Apply generously 15 minutes before sun exposure. Children under 6 months of age: Ask a doctor for sunscreen use

Inactive ingredients

Mica, Methyl Methacrylate Crosspolymer, Aloe Barbadensis Leaf Juice, BHT, Silica, Maris Limus ( Dead sea mineral Mud), CI 77492,Hydrogenated Lecithin, CI 77491, CI 77499.

Questions?

Visit www.noonaesthetics.com or call toll free1-833-666-6246

— FDA label of Brush and Go All Skin types, Noon Aesthetics M.R. Ltd, effective January 13, 2025. See the official label on DailyMed →

BRUSH and GO SPF 50 ALL SKIN TYPES BROAD SPECTRUM · Noon Aesthetics M.R. Ltd

Avobenzone 0.045 g/5 mL · Octinoxate 0.141 g/5 mL · Octisalate 0.08 g/5 mL · Octocrylene 0.135 g/5 mL · Oxybenzone 0.045 g/5 mL · Titanium dioxide 0.75 g/5 mL, powder (topical)

Active ingredient

/ Purpose: Titanium Dioxide 25% Sunscreen Ethylhexyl Methoxycinnamate 4.7% Sunscreen Octocrylene 4.5% Sunscreen Ethylhexyl Salicylate 2.7% Sunscreen Butyl Methoxydibenzoylmethane 1.5% Sunscreen Benzophenone 1.5% Sunscreen

Purpose

Active Ingredients / Purpose: Titanium Dioxide 25% Sunscreen Ethylhexyl Methoxycinnamate 4.7% Sunscreen Octocrylene 4.5% Sunscreen Ethylhexyl Salicylate 2.7% Sunscreen Butyl Methoxydibenzoylmethane 1.5% Sunscreen Benzophenone 1.5% Sunscreen

Uses

Helps prevent sunburn.

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 or irritation develops and lasts.

Keep out of reach of children

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

Directions

Apply liberally 15 minutes before sun exposure and as needed. Use a water-resistant sunscreen if swimming or sweating. Reapply at least every 2 hours. Children under 6 months: Ask a doctor. 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.

Inactive ingredients

Mica, Methyl Methacrylate Crosspolymer, Magnesium Stearate, Silica, CI 77492, CI 77491, CI 77499, Silt (Dead Sea Mineral Mud), Aloe Barbadensis Leaf Juice, Tin Oxide, Hydrogenated Lecithin, Phenoxyethanol, BHT, Caprylyl Glycol

Questions?

Visit www.noonaesthetics.com or call toll free1-833-666-6246

— FDA label of BRUSH and GO SPF 50 ALL SKIN TYPES BROAD SPECTRUM, Noon Aesthetics M.R. Ltd, effective January 16, 2026. See the official label on DailyMed →

This page is not medical advice. Read the label on your package, and ask a pharmacist or doctor if you are not sure a medicine is right for you, for your child, or with your other medicines.

Same medicine, other brands

Each group lists the products that have exactly the same active ingredients, in the same amount and form, as registered with the FDA (NDC Directory). A store brand in the same group has the same medicine as the name brand; inactive ingredients, flavors and package sizes can differ. Each product links to its own official label.

Avobenzone 0.075 g/5 g · Octinoxate 0.236 g/5 g · Octisalate 0.135 g/5 g · Octocrylene 0.225 g/5 g · Oxybenzone 0.075 g/5 g · Titanium dioxide 1.25 g/5 g · powder (topical) · 6 products

Drug Facts for this strength and form ↑

Brand or product nameCompany on the labelLabel
Brush and Go All Skin types Noon Aesthetics M.R. Ltd DailyMed
Brush and Go All Skin types Matte Finish Tone 1 Noon Aesthetics M.R. Ltd DailyMed
Brush and Go All Skin types Matte Finish Tone 2 Noon Aesthetics M.R. Ltd DailyMed
Brush and Go Oily Problematic Skin Noon Aesthetics M.R. Ltd DailyMed
Brush and Go Oily Problematic Skin Matte Finish Tone 1 Noon Aesthetics M.R. Ltd DailyMed
Brush and Go Oily Problematic Skin Matte Finish Tone 2 Noon Aesthetics M.R. Ltd DailyMed
Avobenzone 0.045 g/5 mL · Octinoxate 0.141 g/5 mL · Octisalate 0.08 g/5 mL · Octocrylene 0.135 g/5 mL · Oxybenzone 0.045 g/5 mL · Titanium dioxide 0.75 g/5 mL · powder (topical) · 2 products

Drug Facts for this strength and form ↑

Brand or product nameCompany on the labelLabel
BRUSH and GO SPF 50 ALL SKIN TYPES BROAD SPECTRUM Noon Aesthetics M.R. Ltd DailyMed
BRUSH and GO SPF 50 OILY/PROBLEMATIC SKIN BROAD SPECTRUM Noon Aesthetics M.R. Ltd DailyMed

Companies that sell this medicine

The company named on the package (maker or distributor), as listed in the FDA NDC Directory, with its number of over-the-counter products of this medicine.

  • Noon Aesthetics M.R. Ltd8 products

Recalls

No recall linked to these products (by their NDC code or label) appears in the FDA enforcement reports.

Next steps

Sources

  1. Drug labeling (SPL, openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  2. NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  3. Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
  4. FDA rule for the Drug Facts label (21 CFR 201.66)

Only medicines marketed under FDA rules for nonprescription drugs (an FDA monograph or an FDA approval) are listed. Homeopathic products are not listed: the FDA does not evaluate them for safety or effectiveness.

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