Label: LUMINOUS AQUA SUNSCREEN MIST- avobenzone, homosalate, octisalate, octocrylene spray
- NDC Code(s): 84326-724-01
- Packager: RBGROUP Co., Ltd
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 21, 2025
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- DO NOT USE
- WHEN USING
- KEEP OUT OF REACH OF CHILDREN
- STOP USE
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DOSAGE & ADMINISTRATION
Directions
● Spray liberally and spread evenly by hand 15 minutes before sun exposure.
● Apply to all skin exposed to the sun.
● Do not spray directly into face.
● Spray on hands and then apply to face. Rub in.
● If bothersome dryness or peeling occurs, reduce application to once a day or every other day.
● Do not apply in windy conditions.
● Reapply at least every 2 hours.
● 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 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-sleeve shirts, pants, hats, and sunglasses.
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INACTIVE INGREDIENT
Alcohol, Isopropyl Myristate, Butyloctyl Salicylate, Acrylates/Octylacrylamide Copolymer, Water, Benzyl Glycol, Ethylhexylglycerin, 1,2-Hexanediol, Glycerin, Butylene Glycol, Sodium Hyaluronate, Ethyl Hexanediol, Centella Asiatica Extract, Madecassic Acid, Asiaticoside, Aslatic Acid, Hydrolyzed Hyaluronic Acid, Sodium Acetylated Hyaluronate, Fragrance
- WARNINGS
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
LUMINOUS AQUA SUNSCREEN MIST
avobenzone, homosalate, octisalate, octocrylene sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84326-724 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 9.5 g in 100 g AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 2.8 g in 100 g OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 4.8 g in 100 g HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 7.3 g in 100 g Inactive Ingredients Ingredient Name Strength MADECASSIC ACID (UNII: M7O1N24J82) ALCOHOL (UNII: 3K9958V90M) BENZYL GLYCOL (UNII: 06S8147L47) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) ETHYL HEXANEDIOL (UNII: M9JGK7U88V) ASIATICOSIDE (UNII: PKO39VY215) ASIATIC ACID (UNII: 9PA5A687X5) SODIUM ACETYLATED HYALURONATE (UNII: WN66R7GL93) HYALURONIC ACID (UNII: S270N0TRQY) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) WATER (UNII: 059QF0KO0R) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) SODIUM HYALURONATE (UNII: YSE9PPT4TH) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) ACRYLATES/OCTYLACRYLAMIDE COPOLYMER (40000 MW) (UNII: 7LL6SY9YFV) GLYCERIN (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:84326-724-01 1 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 12/23/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 12/23/2024 Labeler - RBGROUP Co., Ltd (987610097) Establishment Name Address ID/FEI Business Operations reBom Co., Ltd 695951708 manufacture(84326-724)

