Label: TOO FACED HANGOVER GOOD TO GO SPF 25 BROAD SPECTRUM MOISTURIZER- avobenzone, homosalate, octisalate, and octocrylene lotion
- NDC Code(s): 79596-005-01
- Packager: TOO FACED COSMETICS LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 12, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Use
- Warnings
-
Directions
For sunscreen use:
- apply generously and evenly 15 minutes before sun exposure
- reapply at least every two 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
-
Inactive ingredients
Water\Aqua\Eau, C12-15 Alkyl Benzoate, Glycerin, Octyldodecyl Neopentanoate, Butylene Glycol, Glyceryl Stearate, PEG-100 Stearate, Tocopheryl Acetate, Sodium Hyaluronate, Aloe Barbadensis Leaf Extract, Cinnamomum Zeylanicum Bark Extract, Simmondsia Chinensis (Jojoba) Seed Oil, Sodium Acetate, Beeswax\Cera Alba\Cire D'abeille, Ethylhexylglycerin, Inulin, Lactobacillus Ferment, Octyldodecanol, Sarcosine, Yogurt Powder, Cellulose, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Capryloyl Glycine, Steareth-20, Hydroxyethylcellulose, Hexylene Glycol, Citric Acid, Sodium Hydroxide, Fragrance (Parfum), Cocos Nucifera (Coconut) Water, Disodium EDTA, Tetrahexyldecyl Ascorbate, Phenoxyethanol, Potassium Sorbate, Sodium Benzoate <ILN45850>
- Other information
- Questions?
- PRINCIPAL DISPLAY PANEL - 40 mL Tube Carton
-
INGREDIENTS AND APPEARANCE
TOO FACED HANGOVER GOOD TO GO SPF 25 BROAD SPECTRUM MOISTURIZER
avobenzone, homosalate, octisalate, and octocrylene lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79596-005 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 30 mg in 1 mL HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 80 mg in 1 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 50 mg in 1 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 80 mg in 1 mL Inactive Ingredients Ingredient Name Strength ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) PEG-100 STEARATE (UNII: YD01N1999R) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) HYALURONATE SODIUM (UNII: YSE9PPT4TH) ALOE VERA LEAF (UNII: ZY81Z83H0X) CINNAMON BARK OIL (UNII: XE54U569EC) JOJOBA OIL (UNII: 724GKU717M) SODIUM ACETATE (UNII: 4550K0SC9B) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) INULIN (UNII: JOS53KRJ01) LIMOSILACTOBACILLUS REUTERI (UNII: 9913I24QEE) OCTYLDODECANOL (UNII: 461N1O614Y) SARCOSINE (UNII: Z711V88R5F) POWDERED CELLULOSE (UNII: SMD1X3XO9M) CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO) CAPRYLOYL GLYCINE (UNII: 8TY5YO42NJ) STEARETH-20 (UNII: L0Q8IK9E08) HEXYLENE GLYCOL (UNII: KEH0A3F75J) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) SODIUM HYDROXIDE (UNII: 55X04QC32I) COCONUT WATER (UNII: 267F5Y81NT) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ) PHENOXYETHANOL (UNII: HIE492ZZ3T) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) SODIUM BENZOATE (UNII: OJ245FE5EU) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79596-005-01 1 in 1 CARTON 06/15/2019 1 40 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 06/15/2019 Labeler - TOO FACED COSMETICS LLC (014131481) Registrant - Estee Lauder Companies Inc. (790802086) Establishment Name Address ID/FEI Business Operations MANA PRODUCTS, INC 078870292 manufacture(79596-005)