Label: ABIB AIRY CLEAR SUNSCREEN GEL SMOOTHING TUBE- homosalate, octocrylene, octisalate, avobenzone gel
- NDC Code(s): 73676-100-01, 73676-100-02
- Packager: Fourcompany Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 10, 2025
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- DO NOT USE
- STOP USE
- WHEN USING
- KEEP OUT OF REACH OF CHILDREN
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DOSAGE & ADMINISTRATION
Directions
1.Apply liberally and evenly 15 minutes before sun exposure. Reapply at least every two hours
2.Use a water-resistant sunscreen if swimming or sweating
3.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 sunglasses4.Children under 6 months of age: Ask a doctor
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INACTIVE INGREDIENT
Inactive Ingredient
Isododecane, Butyloctyl Salicylate, Dimethicone/Bis-Isobutyl PPG-20 Crosspolymer, Dextrin Palmitate, Dibutyl Adipate, Methyl Methacrylate Crosspolymer, Acrylates Copolymer, Benzotriazolyl Dodecyl p-Cresol, Polyphenylsilsesquioxane, Trimethylsiloxysilicate, Cedrus Atlantica Bark Oil, Tocopherol, Cananga Odorata Flower Oil, Glycerin, Squalane, Tocopheryl Acetate, Jasminum
Officinale (Jasmine) Oil, Ectoin, Sodium Hyaluronate - Warnings
- Uses
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
ABIB AIRY CLEAR SUNSCREEN GEL SMOOTHING TUBE
homosalate, octocrylene, octisalate, avobenzone gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73676-100 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 65 mg in 1 mL AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 28 mg in 1 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 80 mg in 1 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 45 mg in 1 mL Inactive Ingredients Ingredient Name Strength METHYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER (UNII: EG97988M5Q) GLYCERIN (UNII: PDC6A3C0OX) ISODODECANE (UNII: A8289P68Y2) DIMETHICONE/BIS-ISOBUTYL PPG-20 CROSSPOLYMER (UNII: O4I3UFO6ZF) DEXTRIN PALMITATE (CORN; 20000 MW) (UNII: 89B2BSF9I3) DIBUTYL ADIPATE (UNII: F4K100DXP3) CANANGA ODORATA FLOWER OIL (UNII: 8YOY78GNNX) POLYPHENYLSILSESQUIOXANE (RI 1.55) (UNII: HCT9WH7ZV9) ECTOINE (UNII: 7GXZ3858RY) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) SQUALANE (UNII: GW89575KF9) BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW) (UNII: JZ1374NL9E) JASMINUM OFFICINALE FLOWER (UNII: 0Q8K841432) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) SODIUM HYALURONATE (UNII: YSE9PPT4TH) TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8) (UNII: 5041RX63GN) CEDRUS ATLANTICA BARK OIL (UNII: ZX5QRE4U60) TOCOPHEROL (UNII: R0ZB2556P8) BENZOTRIAZOLYL DODECYL P-CRESOL (UNII: 298PX4M11X) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73676-100-02 1 in 1 BOX 05/30/2025 1 NDC:73676-100-01 30 mL 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 05/30/2025 Labeler - Fourcompany Co., Ltd. (694864584) Registrant - Fourcompany Co., Ltd. (694864584) Establishment Name Address ID/FEI Business Operations COSMAX, INC. 689049693 manufacture(73676-100)

