Skip to main content

BRUSH and GO SPF 50

NDC 78863-3003 · Noon Aesthetics M.R. Ltd

Generic nameTITANIUM DIOXIDE, OCTINOXATE, OCTOCRYLENE, OCTISALATE, AVOBENZONE, and OXYBENZONE
Dosage formPOWDER
RouteTOPICAL
Active ingredient(s)TITANIUM DIOXIDE, OCTINOXATE, OCTOCRYLENE, OCTISALATE, AVOBENZONE, OXYBENZONE
Strength.045; .141; .08; .135; .045; .75 g/5mL; g/5mL; g/5mL; g/5mL; g/5mL; g/5mL
Marketing categoryOTC MONOGRAPH DRUG

Packages

78863-3003-1 — 2 BOTTLE, PLASTIC in 1 CARTON (78863-3003-1) / 5 mL in 1 BOTTLE, PLASTIC

78863-3003-2 — 3 BOTTLE, PLASTIC in 1 CARTON (78863-3003-2) / 5 mL in 1 BOTTLE, PLASTIC

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

78611-4146 — Titanium Dioxide and Zinc Oxide, 78709-001 — Zinc Oxide, Titanium Dioxide, 78709-002 — Zinc Oxide, Titanium Dioxide, 78863-1010 — Titanium Dioxide, Octinoxate, Octocrylene, Octisalate, Avobenzone, and Oxybenzone, 78863-1011 — Titanium Dioxide, Octinoxate, Octocrylene, Octisalate, Avobenzone, and Oxybenzone, 78863-1012 — Titanium Dioxide, Octinoxate, Octocrylene, Octisalate, Avobenzone, and Oxybenzone, 78863-1013 — Titanium Dioxide, Octinoxate, Octocrylene, Octisalate, Avobenzone, and Oxybenzone, 78863-1016 — Titanium Dioxide, Octinoxate, Octocrylene, Octisalate, Avobenzone, and Oxybenzone, 78863-1017 — Titanium Dioxide, Octinoxate, Octocrylene, Octisalate, Avobenzone, and Oxybenzone, 78863-1110 — Titanium Dioxide, Octocrylene, and Avobenzone, 78863-3004 — TITANIUM DIOXIDE, OCTINOXATE, OCTOCRYLENE, OCTISALATE, AVOBENZONE, and OXYBENZONE, 79214-157 — OCTINOXATE, OCTISALATE, ZINC OXIDE, 79265-8072 — Mineral Sunscreen, 79265-8078 — Zinc Oxide, Titanium Dioxide, 79481-0001 — Avbenzone, Octisalate, Octocrylene, 79481-0932 — Avobenzone, Homosalate, Octisalate, 79481-0933 — Avobenzone, Homosalate, Octisalate, 79481-0934 — Avobenzone, Homosalate, Octisalate, 79481-0936 — Avobenzone, Homosalate, Octisalate, 79481-0938 — Avobenzone, Homosalate, Octisalate, Octocrylene, +6199 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels