Label: ISNTREE HYALURONIC ACID DAILY SUNGEL- avobenzone, homosalate, octisalate cream
- NDC Code(s): 81100-501-01, 81100-501-02
- Packager: ISNTREE Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated April 3, 2024
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- Official Label (Printer Friendly)
- Active ingredients
- Purpose
- Uses
- Warnings
- Do not use
- When using this product
- Stop use and ask a doctor if
- Keep out of reach of children
-
Directions
■ apply liberally 15 minutes before sun exposure.
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
■ reapply at least every 2 hours.
■ use a water-resistant sunscreen if swimming or sweating.
- Other information
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Inactive ingredients
Water, Butyloctyl Salicylate, Butylene Glycol, Diethylhexyl 2,6-Naphthalate, Niacinamide, C20-22 Alkyl Phosphate, C20-22 Alcohols, 1,2-Hexanediol, Pentylene Glycol, Acrylates Copolymer, Polymethylsilsesquioxane, Cetyl Alcohol, Poly C10-30 Alkyl Acrylate, VP/Eicosene Copolymer, Glyceryl Stearate, Silica, Tromethamine, Propanediol, Polyacrylate Crosspolymer-6, Xanthan Gum, Ethylhexylglycerin, Adenosine, Portulaca Oleracea Extract, Centella Asiatica Extract, Houttuynia Cordata Extract, Hydrolyzed Hyaluronic Acid, Hydrolyzed Sodium Hyaluronate, Dimethylsilanol Hyaluronate, Hyaluronic Acid, Sodium Hyaluronate, Potassium Hyaluronate, Sodium Hyaluronate Crosspolymer, Hydroxypropyltrimonium Hyaluronate, Sodium Hyaluronate Dimethylsilanol, Sodium Acetylated Hyaluronate, Tocopherol, Ectoin, Dipropylene Glycol, Sodium Palmitoyl Proline, Glycerin, Beta-Glucan, Nymphaea Alba Flower Extract
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ISNTREE HYALURONIC ACID DAILY SUNGEL
avobenzone, homosalate, octisalate creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:81100-501 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 4.5 g in 50 mL AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 1.35 g in 50 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 2.25 g in 50 mL Inactive Ingredients Ingredient Name Strength POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69) XANTHAN GUM (UNII: TTV12P4NEE) ADENOSINE (UNII: K72T3FS567) DIETHYLHEXYL 2,6-NAPHTHALATE (UNII: I0DQJ7YGXM) NIACINAMIDE (UNII: 25X51I8RD4) CETYL ALCOHOL (UNII: 936JST6JCN) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) PROPANEDIOL (UNII: 5965N8W85T) HYALURONIC ACID (UNII: S270N0TRQY) SODIUM PALMITOYL PROLINE (UNII: 64L053FRFO) GLYCERIN (UNII: PDC6A3C0OX) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) SODIUM ACETYLATED HYALURONATE (UNII: WN66R7GL93) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) DIMETHYLSILANOL HYALURONATE (UNII: Z853O1D4TE) HYALURONATE SODIUM (UNII: YSE9PPT4TH) C20-22 ALCOHOLS (UNII: O4M0347C6A) TOCOPHEROL (UNII: R0ZB2556P8) DIPROPYLENE GLYCOL (UNII: E107L85C40) PENTYLENE GLYCOL (UNII: 50C1307PZG) TROMETHAMINE (UNII: 023C2WHX2V) CENTELLA ASIATICA TRITERPENOIDS (UNII: 4YS74Q4G4J) HOUTTUYNIA CORDATA FLOWERING TOP (UNII: RH041UUZ22) PURSLANE (UNII: M6S840WXG5) ECTOINE (UNII: 7GXZ3858RY) WATER (UNII: 059QF0KO0R) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) AMMONIUM ACRYLOYLDIMETHYLTAURATE, DIMETHYLACRYLAMIDE, LAURYL METHACRYLATE AND LAURETH-4 METHACRYLATE COPOLYMER, TRIMETHYLOLPROPANE TRIACRYLATE CROSSLINKED (45000 MPA.S) (UNII: Q7UI015FF9) NYMPHAEA ALBA FLOWER (UNII: 40KQ7Q535O) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) C20-22 ALKYL PHOSPHATE (UNII: L4VKP0Y7RP) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:81100-501-02 1 in 1 BOX 01/17/2024 1 NDC:81100-501-01 50 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 01/17/2024 Labeler - ISNTREE Inc. (689043012) Establishment Name Address ID/FEI Business Operations Kolmar Korea Co.,LTD. Gwanjeong 2 factory 963271750 manufacture(81100-501)