Label: CHARDONNAY LIP OIL- avobenzone homosalate octisalate octocrylene oil
- NDC Code(s): 80641-012-92, 80641-012-93
- Packager: Vacation Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated March 13, 2024
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- Official Label (Printer Friendly)
- Dosage and Administration
- Warnings
- Indications and Usage
- Keep out of reach of children
- Purpose
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Inactives
Butyloctyl Salicylate, Butyrospermum Parkii (Shea) Butter, Caprylic/Capric Triglyceride, Capryloyl Glycerin/Sebacic Acid Copolymer, Cetearly Ethylhexanoate, Ethyl Ferulate, Flavor, Glyceryl, Behenate, HDI/Trimethylol Hexyllactone Crosspolymer, Hydrogenated Poly (C6-20 Olefin), Hydrolyzed Sodium Hyaluyronate, Limnanthes Alba (Meadowfoam) Seed Oil, Palmitoyl Tripeptide-38, Polyester-8, Polyglyceryl-2 Isostearate/Dimer Dilinoleate Copolymer, Portulaca Pilosa Extract, Prunus Avium (Sweet Cherry) Seed Oil, Silica Silylate, Sorbitan Isostearate, Soybean Glycerides, Stevia Rebaudiana Extract, Sucrose Cocoate, Tetrahexyldecyl Ascorbate (Vitamin C), Tocopherol (Vitamin E), Trimethylpentanediol/Adipic Acid/Glycerin Crosspolymer, Vitis Vinifera (Grape) Seed Oil
- Chardonnay Lip Oil
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INGREDIENTS AND APPEARANCE
CHARDONNAY LIP OIL
avobenzone homosalate octisalate octocrylene oilProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:80641-012 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 5 g in 100 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 8 g in 100 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 4.9 g in 100 mL AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 2.9 g in 100 mL Inactive Ingredients Ingredient Name Strength BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:80641-012-92 8.6 mL in 1 VIAL; Type 0: Not a Combination Product 03/07/2024 2 NDC:80641-012-93 5.9 mL in 1 VIAL; Type 0: Not a Combination Product 03/07/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 03/07/2024 Labeler - Vacation Inc (117644631)