CLEAR SYSTEM BRIGHTENING DAY CREAM SPF 15- octocrylene, octisalate cream

Clear System Brightening Day Cream by

Drug Labeling and Warnings

Clear System Brightening Day Cream by is a Otc medication manufactured, distributed, or labeled by Bentley Laboratories, LLC, Geologie. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

DRUG FACTS

Active Ingredients

Octocrylene 5%

Octisalate 2%

PURPOSE

Purpose

Octocrylene ....... Sunscreen

Octisalate .......... Sunscreen

INDICATIONS & USAGE

Uses Helps prevent sunburn if used as directed with other sun protection measures (see Directions) decreases the
risk of skin cancer and early signs of aging from the sun.

WARNINGS

Warnings For external use only.  Do not use on damaged or broken skin.  When using this product keep

out of eyes. Rinse with water to remove. Stop use and ask doctor if rash occurs.

KEEP OUT OF REACH OF CHILDREN

Keep out of the reach of children. If swallowed get medical help

or contact a Poison Control center right away.

DOSAGE & ADMINISTRATION

Directions  ​​ Use in the morning.  Rub cream gently into your entire face and neck, avoiding the eyes.

INACTIVE INGREDIENT

Inactive Ingredients Aloe Barbadensis Leaf Juice, Water, Butyloctyl Salicylate, Cetearyl Olivate, Sorbitan
Olivate, Glyceryl Stearate, Potassium Azeloyl Diglycinate, Glycerin, Niacinamide, Polyglyceryl-10 Laurate, Sodium
Hyaluronate, Silica, Caffeine, Phenoxyethanol, Caprylyl Glycol, Dimethicone, Sodium Stearoyl Glutamate, Hydroxy-
ethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Ethyl Ferulate, Ethylhexylglycerin, Arnica Montana
Flower Extract

Geologie Clear System Brightening Day Cream

PERSONALIZED SKINCARE

Clear System Brightening Day Cream SPF 15

Geologie.com
Made in USA of
Imported Materials
Distributed by Geologie
New York, NY 10025

20 mL Tube

40 mL Tube

60 mL Tube

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INGREDIENTS AND APPEARANCE

CLEAR SYSTEM BRIGHTENING DAY CREAM  SPF 15
octocrylene, octisalate cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 54111-187
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	5.0 g  in 100 mL
OCTISALATE (UNII: 4X49Y0596W) (ETHYLHEXYL SALICYLATE - UNII:4X49Y0596W)	OCTISALATE	2.0 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE BARBADENSIS LEAF JUICE (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
CETEARYL OLIVATE (UNII: 58B69Q84JO)
SORBITAN OLIVATE (UNII: MDL271E3GR)
GLYCERYL STEARATE (UNII: 230OU9XXE4)
POTASSIUM AZELOYL DIGLYCINATE (UNII: N02RVN6NYP)
GLYCERIN (UNII: PDC6A3C0OX)
NIACINAMIDE (UNII: 25X51I8RD4)
POLYGLYCERYL-10 LAURATE (UNII: MPJ2Q8WI8G)
SODIUM HYALURONATE (UNII: YSE9PPT4TH)
SILICA (UNII: ETJ7Z6XBU4)
CAFFEINE (UNII: 3G6A5W338E)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
DIMETHICONE (UNII: 92RU3N3Y1O)
SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024)
HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%) (UNII: 86FQE96TZ4)
ETHYL FERULATE (UNII: 5B8915UELW)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 54111-187-20	20 mL in 1 TUBE; Type 0: Not a Combination Product	12/01/2024
2	NDC: 54111-187-40	40 mL in 1 TUBE; Type 0: Not a Combination Product	12/01/2024
3	NDC: 54111-187-60	60 mL in 1 TUBE; Type 0: Not a Combination Product	12/01/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	12/01/2024

Labeler - Bentley Laboratories, LLC (068351753)

Registrant - Geologie (081158549)