Label: KIEHLS SINCE 1851 FACIAL FUEL DAILY ENERGIZING MOISTURE TREATMENT FOR MEN BROAD SPECTRUM SPF 20 SUNSCREEN- avobenzone, homosalate, octisalate and octocrylene lotion
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NDC Code(s):
49967-608-01,
49967-608-02,
49967-608-03,
49967-608-04, view more49967-608-05
- Packager: L'Oreal USA Products Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 30, 2023
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- Official Label (Printer Friendly)
- Active ingredients
- Purpose
- Uses
- Warnings
- Do not use
- When using this product
- Stop use and ask a doctor if
- Keep out of reach of children.
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Directions
For sunscreen use:
● apply liberally 15 minutes before sun exposure
● reapply at least every 2 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
- Other information
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Inactive ingredients
water, dimethicone, glycerin, alcohol denat., tocopherol, aloe barbadensis leaf juice, phenoxyethanol, sodium hydroxide, caprylyl glycol, sodium polyacrylate, fragrance, acrylates/c10-30 alkyl acrylate crosspolymer, ascorbyl glucoside, acrylates/dimethicone copolymer, caffeine, sodium hyaluronate, xanthan gum, menthyl lactate, disodium EDTA, limonene, ceramide NP, castanea sativa (chestnut) seed extract, pentylene glycol, hydrolyzed soy protein, linalool, citric acid, potassium sorbate, citral, sodium benzoate, ethylhexylglycerin
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- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
KIEHLS SINCE 1851 FACIAL FUEL DAILY ENERGIZING MOISTURE TREATMENT FOR MEN BROAD SPECTRUM SPF 20 SUNSCREEN
avobenzone, homosalate, octisalate and octocrylene lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49967-608 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 88 mg in 1 mL Octisalate (UNII: 4X49Y0596W) (Octisalate - UNII:4X49Y0596W) Octisalate 49 mg in 1 mL Octocrylene (UNII: 5A68WGF6WM) (Octocrylene - UNII:5A68WGF6WM) Octocrylene 59 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) DIMETHICONE (UNII: 92RU3N3Y1O) ALCOHOL (UNII: 3K9958V90M) TOCOPHEROL (UNII: R0ZB2556P8) ALOE VERA LEAF (UNII: ZY81Z83H0X) PHENOXYETHANOL (UNII: HIE492ZZ3T) SODIUM HYDROXIDE (UNII: 55X04QC32I) CAPRYLYL GLYCOL (UNII: 00YIU5438U) SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L) CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO) ASCORBYL GLUCOSIDE (UNII: 2V52R0NHXW) CAFFEINE (UNII: 3G6A5W338E) HYALURONATE SODIUM (UNII: YSE9PPT4TH) XANTHAN GUM (UNII: TTV12P4NEE) METHYL LACTATE, (-)- (UNII: 0379G9C44S) EDETATE DISODIUM (UNII: 7FLD91C86K) LIMONENE, (+)- (UNII: GFD7C86Q1W) CERAMIDE NP (UNII: 4370DF050B) SPANISH CHESTNUT (UNII: 2MT5XMR2YW) PENTYLENE GLYCOL (UNII: 50C1307PZG) HYDROLYZED SOY PROTEIN (ENZYMATIC; 2000 MW) (UNII: 1394NXB9L6) LINALOOL, (+/-)- (UNII: D81QY6I88E) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) CITRAL (UNII: T7EU0O9VPP) SODIUM BENZOATE (UNII: OJ245FE5EU) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49967-608-01 1 in 1 CARTON 03/29/2018 1 125 mL in 1 TUBE; Type 0: Not a Combination Product 2 NDC:49967-608-02 1 in 1 CARTON 03/29/2018 2 15 mL in 1 TUBE; Type 0: Not a Combination Product 3 NDC:49967-608-03 1 in 1 CARTON 12/10/2018 3 75 mL in 1 TUBE; Type 0: Not a Combination Product 4 NDC:49967-608-04 1 in 1 CARTON 12/10/2018 4 200 mL in 1 TUBE; Type 0: Not a Combination Product 5 NDC:49967-608-05 3 mL in 1 PACKET; Type 0: Not a Combination Product 12/10/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 03/29/2018 Labeler - L'Oreal USA Products Inc (002136794) Establishment Name Address ID/FEI Business Operations L'Oreal USA Products Inc 185931458 manufacture(49967-608) , pack(49967-608)
