BRUSH AND GO SPF 50 ALL SKIN TYPES BROAD SPECTRUM- titanium dioxide, octinoxate, octocrylene, octisalate, avobenzone, and oxybenzone powder

BRUSH and GO SPF 50 by

Drug Labeling and Warnings

BRUSH and GO SPF 50 by is a Otc medication manufactured, distributed, or labeled by Noon Aesthetics M.R. Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

DRUG FACTS INFORMATION

ACTIVE INGREDIENT

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.

Other Information

• Sun alert: Limiting sun exposure, wearing protective clothing, and using sunscreens may reduce the risks of skin aging, skin cancer, and other harmful effects of the sun.

Questions or comments?

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

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

SPL UNCLASSIFIED SECTION

Developed + Dist by
noon AESTHETICS
TLV, 62153

PRINCIPAL DISPLAY PANEL - 5 mL Bottle Carton

no
on
AESTHETICS

Brush & Go™
SPF 50

BROAD-SPECTRUM

ALL SKIN TYPES

NDC: 78863-3003-1

2 X 5 mL / 0.17 Fl. Oz. ℮

INGREDIENTS AND APPEARANCE

BRUSH AND GO SPF 50   ALL SKIN TYPES BROAD SPECTRUM
titanium dioxide, octinoxate, octocrylene, octisalate, avobenzone, and oxybenzone powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78863-3003
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	0.75 g  in 5 mL
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	0.141 g  in 5 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	0.135 g  in 5 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	0.08 g  in 5 mL
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	0.045 g  in 5 mL
OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y)	OXYBENZONE	0.045 g  in 5 mL

Inactive Ingredients
Ingredient Name	Strength
MICA (UNII: V8A1AW0880)
METHYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER (UNII: EG97988M5Q)
MAGNESIUM STEARATE (UNII: 70097M6I30)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
FERRIC OXIDE RED (UNII: 1K09F3G675)
FERROSOFERRIC OXIDE (UNII: XM0M87F357)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
STANNOUS OXIDE (UNII: JB2MV9I3LS)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)

Product Characteristics
Color	BROWN (LIGHT BROWN)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78863-3003-1	2 in 1 CARTON	04/01/2024
1		5 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
2	NDC: 78863-3003-2	3 in 1 CARTON	04/01/2024
2		5 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph drug	M020	04/01/2024

Labeler - Noon Aesthetics M.R. Ltd (600185560)

Establishment
Name	Address	ID/FEI	Business Operations
Noon Aesthetics M.R. Ltd		600185560	MANUFACTURE(78863-3003)