Label: AESOP AVAIL FACIAL SUNSCREEN BROAD SPECTRUM SPF 25- avobenzone, homosalate, octisalate, octocrylene lotion
- NDC Code(s): 76293-928-01
- Packager: Emeis Cosmetics Pty Ltd
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 17, 2025
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- Official Label (Printer Friendly)
- Active ingredients
- Purpose
-
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.
- Warnings
-
Directions
For sunscreen use:
- apply generously 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 - Other information
-
Inactive ingredients
water, coco-caprylate/caprate, tribehenin
PEG-20 esters, glycerin, copernicia
cerifera (carnauba) wax, silica,
ethylhexylglycerin, caprylic/capric
triglyceride, phenoxyethanol, benzyl
alcohol, glycine soja (soybean) oil,
tocopherol, panthenol, lavandula
angustifolia (lavender) oil, acrylates/
C10-30 alkyl acrylate crosspolymer,
rosmarinus officinalis (rosemary)
leaf oil, sodium stearoyl glutamate,
trisodium ethylenediamine disuccinate,
microcrystalline cellulose, sodium
dehydroacetate, tocopheryl acetate,
cedrus atlantica (cedarwood) bark
oil, sodium hydroxide, cellulose gum,
sodium carrageenan, camellia sinensis
leaf extract, sea salt (maris sal), lactic
acid, sodium benzoate, beta-carotene,
daucus carota sativa (carrot) root extract,
potassium sorbate, linalool, limonene,
geraniol - PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
AESOP AVAIL FACIAL SUNSCREEN BROAD SPECTRUM SPF 25
avobenzone, homosalate, octisalate, octocrylene lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76293-928 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 30.0 mg in 1 g HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 70.0 mg in 1 g OCTISALATE (UNII: 4X49Y0596W) (ETHYLHEXYL SALICYLATE - UNII:4X49Y0596W) OCTISALATE 40.0 mg in 1 g OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 70.0 mg in 1 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H) TRIBEHENIN PEG-20 ESTERS (UNII: 84K9EH29Y9) GLYCERIN (UNII: PDC6A3C0OX) COPERNICIA CERIFERA (CARNAUBA) WAX (UNII: R12CBM0EIZ) SILICA (UNII: ETJ7Z6XBU4) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) CAPRYLIC/CAPRIC TRIGLYCERIDE (UNII: C9H2L21V7U) PHENOXYETHANOL (UNII: HIE492ZZ3T) BENZYL ALCOHOL (UNII: LKG8494WBH) SOYBEAN OIL (UNII: 241ATL177A) TOCOPHEROL (UNII: R0ZB2556P8) PANTHENOL (UNII: WV9CM0O67Z) LAVANDULA ANGUSTIFOLIA (LAVENDER) OIL (UNII: ZBP1YXW0H8) ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V) ROSMARINUS OFFICINALIS (ROSEMARY) LEAF OIL (UNII: 8LGU7VM393) SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024) TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) SODIUM DEHYDROACETATE (UNII: 8W46YN971G) .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N) CEDRUS ATLANTICA BARK OIL (UNII: ZX5QRE4U60) SODIUM HYDROXIDE (UNII: 55X04QC32I) CELLULOSE GUM (UNII: K679OBS311) SODIUM CARRAGEENAN (UNII: 7CY8BVL34N) GREEN TEA LEAF (UNII: W2ZU1RY8B0) SEA SALT (UNII: 87GE52P74G) LACTIC ACID, DL- (UNII: 3B8D35Y7S4) SODIUM BENZOATE (UNII: OJ245FE5EU) BETA-CAROTENE (UNII: 01YAE03M7J) CARROT (UNII: L56Z1JK48B) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) LINALOOL (UNII: D81QY6I88E) LIMONENE, (+/-)- (UNII: 9MC3I34447) GERANIOL (UNII: L837108USY) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76293-928-01 1 in 1 CARTON 10/01/2025 1 47.5 g in 1 TUBE; 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 10/01/2025 Labeler - Emeis Cosmetics Pty Ltd (754271146) Establishment Name Address ID/FEI Business Operations Ensign Laboratories Proprietary Limited 753228022 manufacture(76293-928)
