CABANACLEAR ILLUMINATING SPF 50- homosalate, octisalate, avobenzone lotion

CabanaClear Illuminating by

Drug Labeling and Warnings

CabanaClear Illuminating by is a Otc medication manufactured, distributed, or labeled by NAKED SUNDAYS PTY LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredients (% W/W): Avobenzone 3%, Homosalate 6%, Octyl Salicylate 5%

PURPOSE

Sunscreen

INDICATIONS & USAGE

Use:

Helps prevent sunburn.

If used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin ageing caused by the sun

WARNINGS

Warnings: For external use only.

Do not use on damaged or broken skin.

WHEN USING

When using this product: Keep out of eyes. Rinse with water to remove.

STOP USE

Stop use and ask a doctor: If rash occurs.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children: If product is swallowed, get medical help or contact a Poison Control Center right away

DOSAGE & ADMINISTRATION

Directions:

Shake well before use.

Apply liberally and evenly 20 minutes before sun exposure.

Re-apply every 2 hours or immediately after swimming, sweating or towel drying.

Use a water-resistant sunscreen if swimming or sweating.

Children under 6 months of age: 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 10.00AM - 2.00PM

Wear long-sleeved shirts, pants, hats, and sunglasses

OTHER SAFETY INFORMATION

Other Information:

Protect this product from excess heat and direct sun.

Store below 30°C / 86°F

Questions:

info@nakedSundays.com

INACTIVE INGREDIENT

Inactive Ingredients: Water, Butyloctyl Salicylate, Propylene Glycol, Acrylates Copolymer, Euphorbia Cerifera (Candelilla) Wax, Phenoxyethanol, Hydroxyacetophenone, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Polyacrylate Crosspolymer-6, Tocopheryl Acetate, Sodium Hyaluronate, Ethylhexylglycerin, Sodium Hydroxide, Disodium EDTA, Silica, t-Butyl Alcohol, Citric Acid, Sodium Benzoate, Tocopherol, Centella Asiatica Extract, Titanium Dioxide (CI 77891), Mica (CI 77019), Iron Oxide (CI 77491, CI 77492, CI 77499), Tin Oxide (CI 77861)

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

CABANACLEAR ILLUMINATING  SPF 50
homosalate, octisalate, avobenzone lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81104-594
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	5 g  in 100 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	6 g  in 100 mL
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	3 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V)
SILICA (UNII: ETJ7Z6XBU4)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
EUPHORBIA CERIFERA (CANDELILLA) WAX (UNII: WL0328HX19)
EDETATE DISODIUM (UNII: 7FLD91C86K)
MICA (UNII: V8A1AW0880)
CI 77491 (UNII: 1K09F3G675)
CI 77492 (UNII: EX438O2MRT)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
CITRIC ACID (UNII: 2968PHW8QP)
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
POLYACRYLATE CROSSPOLYMER-6 (UNII: Q7UI015FF9)
WATER (UNII: 059QF0KO0R)
SODIUM BENZOATE (UNII: OJ245FE5EU)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW) (UNII: JZ1374NL9E)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
SODIUM HYALURONATE (UNII: YSE9PPT4TH)
CENTELLA ASIATICA TRITERPENOIDS (UNII: 4YS74Q4G4J)
CI 77891 (UNII: 15FIX9V2JP)
CI 77499 (UNII: XM0M87F357)
TIN OXIDE (UNII: KM7N50LOS6)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81104-594-01	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/19/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	12/19/2025

Labeler - NAKED SUNDAYS PTY LTD (746918845)