CLINIQUE FOR MEN BROAD SPECTRUM SPF 21 MOISTURIZER- avobenzone, octinoxate, octisalate, and oxybenzone lotion 
CLINIQUE LABORATORIES LLC

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CLINIQUE FOR MEN BROAD SPECTRUM SPF 21 MOISTURIZER

Drug Facts

Active ingredients

Avobenzone 3.0%
Octinoxate 7.4%
Octisalate 5.0%
Oxybenzone 2.0%

Purpose

Sunscreen

Use

helps prevent sunburn

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 a doctor if rash occurs

Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

Directions

For sunscreen use:

Inactive ingredients

water\aqua\eau•butylene glycol•dimethicone•neopentyl glycol diheptanoate•cetearyl alcohol•peg-100 stearate•silica•hordeum vulgare (barley) extract\extrait d'orge•algae extract•cucumis sativus (cucumber) fruit extract•helianthus annuus (sunflower) seedcake•cholesterol•cetearyl glucoside•propylene glycol dicaprate•tridecyl trimellitate•hydrogenated lecithin•stearyl alcohol•zeolite•lactobacillus ferment•cetrimonium chloride•tridecyl stearate•isododecane•dipentaerythrityl hexacaprylate/hexacaprate•pvp•oleth-10•laureth-4•laureth-23•caprylyl glycol•hexylene glycol•polyethylene•tromethamine•carbomer•sodium citrate•disodium edta•potassium sorbate•phenoxyethanol•yellow 5 (ci 19140)•yellow 6 (ci 15985)•red 33 (ci 17200) [iln43259]

Other information

protect the product in this container from excessive heat and direct sun

PRINCIPAL DISPLAY PANEL - 100 mL Tube Label

CLINIQUE
FOR MEN

broad
spectrum
SPF 21
moisturizer

3.4 FL.OZ.LIQ./100 ml ℮

PRINCIPAL DISPLAY PANEL - 100 mL Tube Label
CLINIQUE FOR MEN BROAD SPECTRUM SPF 21 MOISTURIZER 
avobenzone, octinoxate, octisalate, and oxybenzone lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49527-081
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE30 mg  in 1 mL
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE74 mg  in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE50 mg  in 1 mL
OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE20 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
AGAR, UNSPECIFIED (UNII: 89T13OHQ2B)  
ZEOLITE A (UNII: Y3NG9WF08W)  
LIMOSILACTOBACILLUS REUTERI (UNII: 9913I24QEE)  
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)  
WATER (UNII: 059QF0KO0R)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
PEG-100 STEARATE (UNII: YD01N1999R)  
SILICA, TRIMETHYLSILYL CAPPED (UNII: VU10KU4B9S)  
BARLEY (UNII: 5PWM7YLI7R)  
CUCUMBER (UNII: YY7C30VXJT)  
HELIANTHUS ANNUUS SEEDCAKE (UNII: 482WYF7XLC)  
CHOLESTEROL (UNII: 97C5T2UQ7J)  
CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)  
PROPYLENE GLYCOL DICAPRATE (UNII: U783H9JHWY)  
TRIDECYL TRIMELLITATE (UNII: FY36J270ES)  
HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)  
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
TRIDECYL STEARATE (UNII: A8OE252M6L)  
ISODODECANE (UNII: A8289P68Y2)  
DIPENTAERYTHRITYL HEXACAPRYLATE/HEXACAPRATE (UNII: 554N82UWVW)  
POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)  
OLETH-10 (UNII: JD797EF70J)  
LAURETH-4 (UNII: 6HQ855798J)  
LAURETH-23 (UNII: N72LMW566G)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
HEXYLENE GLYCOL (UNII: KEH0A3F75J)  
HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)  
TROMETHAMINE (UNII: 023C2WHX2V)  
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)  
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49527-081-011 in 1 CARTON07/21/2021
1100 mL in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02007/21/2021
Labeler - CLINIQUE LABORATORIES LLC (044475127)
Registrant - Estee Lauder Companies Inc. (790802086)
Establishment
NameAddressID/FEIBusiness Operations
The Estee Lauder Inc802599436manufacture(49527-081) , pack(49527-081) , label(49527-081)

Revised: 10/2023
Document Id: 0828eba6-8d0e-9a5a-e063-6394a90a2fca
Set id: 2e9463df-1c71-465f-9820-6cedefe07ad7
Version: 5
Effective Time: 20231020
 
CLINIQUE LABORATORIES LLC