Label: MARY KAY SUNCARE SUNSCREEN SPF 50- avobenzone, homosalate, octisalate, octocrylene, oxybenzone lotion
- NDC Code(s): 51531-3275-4
- Packager: Mary Kay Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Export only
Drug Label Information
Updated December 20, 2023
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- Official Label (Printer Friendly)
- PURPOSE
- Indications:
-
Warnings:
For external use only, not to be swallowed.
If rash or irritation develops, discontinue use.
Avoid use in the eye area.
Keep out of reach of children.
Do not stay too long in the sun, even while using a sunscreen product.
Overexposure to the sun is dangerous.
Avoid excessive sun exposure at peak hours (between 11 a.m. and 3 p.m.).
Keep yourself well covered (hat, clothing, sunglasses).
Contains Benzophenone-3.
-
Directions:
Apply liberally (about 6 teaspoons or 36 grams of sunscreen for the average adult body) at least 15 minutes before sun exposure.
Warning: Reducing this quantity will lower the level of protection significantly.
Re-apply every one to three hours to maintain protection, especially after swimming, toweling, vigorous activities or excessive sweating. -
Ingredients:
AQUA, HOMOSALATE, OCTOCRYLENE, BENZOPHENONE-3, ETHYLHEXYL SALICYLATE,
STYRENE/ACRYLATES COPOLYMER, BUTYLOCTYL SALICYLATE, BUTYL METHOXYDIBENZOYLMETHANE,
BUTYLENE GLYCOL, CETEARYL ALCOHOL, CETETH-20 PHOSPHATE, METHYL TRIMETHICONE,
SILICA, ACRYLATES/DIMETHICONE COPOLYMER, ACRYLATES/C12-22 ALKYL METHACRYLATE COPOLYMER,
ETHYLHEXYL METHOXYCRYLENE, VP/EICOSENE COPOLYMER, BEHENYL ALCOHOL, GLYCERIN,
DICETYL PHOSPHATE, PENTYLENE GLYCOL, DIMETHICONE, TRIMETHYLSILOXYSILICATE,
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER, PHENOXYETHANOL, CAPRYLYL GLYCOL,
TRIETHANOLAMINE, ETHYLENE BRASSYLATE, XANTHAN GUM, PROPYLENE GLYCOL, DISODIUM EDTA,
TOCOPHERYL ACETATE, SORBIC ACID, ISOBUTYL METHYL TETRAHYDROPYRANOL,
EUTERPE OLERACEA FRUIT EXTRACT, ETHYL LINALOOL, METHYLENEDIOXYPHENYL METHYLPROPANAL,
AMMONIUM HYDROXIDE, PHENYLISOHEXANOL, CYCLAMEN ALDEHYDE.
- Principal Display Panel - 118 mL carton
-
INGREDIENTS AND APPEARANCE
MARY KAY SUNCARE SUNSCREEN SPF 50
avobenzone, homosalate, octisalate, octocrylene, oxybenzone lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:51531-3275 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 3 g in 100 mL HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 10 g in 100 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 4.5 g in 100 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 5.5 g in 100 mL OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE 5 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) CETETH-20 PHOSPHATE (UNII: 921FTA1500) METHYL TRIMETHICONE (UNII: S73ZQI0GXM) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) DOCOSANOL (UNII: 9G1OE216XY) VINYLPYRROLIDONE/EICOSENE COPOLYMER (UNII: 035MV9S1C3) ETHYLHEXYL METHOXYCRYLENE (UNII: S3KFG6Q5X8) GLYCERIN (UNII: PDC6A3C0OX) DIHEXADECYL PHOSPHATE (UNII: 2V6E5WN99N) PENTYLENE GLYCOL (UNII: 50C1307PZG) TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8) (UNII: 5041RX63GN) DIMETHICONE (UNII: 92RU3N3Y1O) AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG) PHENOXYETHANOL (UNII: HIE492ZZ3T) CAPRYLYL GLYCOL (UNII: 00YIU5438U) TROLAMINE (UNII: 9O3K93S3TK) ETHYLENE BRASSYLATE (UNII: 9A87HC7ROD) XANTHAN GUM (UNII: TTV12P4NEE) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) EDETATE DISODIUM (UNII: 7FLD91C86K) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) SORBIC ACID (UNII: X045WJ989B) 2-ISOBUTYL-4-METHYLTETRAHYDROPYRAN-4-OL (UNII: VK5ZHH2T3F) 3-(3,4-METHYLENEDIOXYPHENYL)-2-METHYLPROPANAL (UNII: L65EG8H6PA) ACAI (UNII: 46AM2VJ0AW) ETHYL LINALOOL (UNII: SF2JS9GF5T) AMMONIA (UNII: 5138Q19F1X) PHENYLISOHEXANOL (UNII: M56178H183) CYCLAMEN ALDEHYDE (UNII: 4U37UX0E1E) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51531-3275-4 1 in 1 CARTON 03/16/2013 1 118 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 Export only 03/16/2013 07/12/2025 Labeler - Mary Kay Inc. (049994452) Establishment Name Address ID/FEI Business Operations Mary Kay Inc. 103978839 manufacture(51531-3275)
