ILLUSION LUMINOUS GLOW FOUNDATION (1-26)- avobenzone, homosalate, and octisalate lotion
ILLUSION LUMINOUS GLOW FOUNDATION (1-26) by
Drug Labeling and Warnings
ILLUSION LUMINOUS GLOW FOUNDATION (1-26) by is a Otc medication manufactured, distributed, or labeled by Kingdom Animalia, LLC DBA Hourglass Cosmetics, MANA PRODUCTS INC.. Drug facts, warnings, and ingredients follow.
Drug Details [pdf]
- SPL UNCLASSIFIED SECTION
- Active Ingredients
- Purpose
-
Uses
- helps prevent sunburn.
- if used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun.
- Warnings
-
Directions
- Apply liberally 15 minutes before sun exposure.
- Use a water resistant sunscreen if swimming or sweating.
- Reapply at least every 2 hours.
-
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 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-sleeve shirts, pants, hats and sunglasses.
- Children under 6 months: Ask a doctor.
- Other Information
- Questions or comments?
-
Inactive Ingredients
WATER/AQUA, BUTYLOCTYL SALICYLATE, COCONUT ALKANES, DIMETHICONE, TRIBEHENIN, POLYGLYCERYL-4 DIISOSTEARATE/POLYHYDROXYSTEARATE/SEBACATE, DICAPRYLYL ETHER, CETYL ALCOHOL, POLYGLYCERYL-6 POLYRICINOLEATE, SILICA, ETHYLHEXYL PALMITATE, GLYCERIN, OCTYLDODECYL NEOPENTANOATE, SODIUM CHLORIDE, SORBITAN OLEATE, LAURYL POLYGLYCERYL-3 POLYDIMETHYLSILOXYETHYL DIMETHICONE, POLYGLYCERYL-2 ISOSTEARATE, DIMETHICONE/POLYGLYCERIN-3 CROSSPOLYMER, CETEARYL ALCOHOL, DISTEARDIMONIUM HECTORITE, CAPRYLYL GLYCOL, VP/EICOSENE COPOLYMER, ETHYLHEXYLGLYCERIN, POTASSIUM SORBATE, SODIUM BENZOATE, COCOCAPRYLATE/CAPRATE, DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER, GLYCERYL DIBEHENATE, ALUMINUM DIMYRISTATE, TRIETHOXYCAPRYLYLSILANE, CITRIC ACID, DISODIUM STEAROYL GLUTAMATE, GLYCERYL BEHENATE, SILICA DIMETHYL SILYLATE, BUTYLENE GLYCOL, DIPROPYLENE GLYCOL, METHYL SALICYLATE, PHENOXYETHANOL, SODIUM CITRATE, SODIUM HYALURONATE, TOCOPHEROL, HEXYLENE GLYCOL, IRON OXIDES (CI 77491, CI 77492, CI 77499), TITANIUM DIOXIDE (CI 77891).
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 35 mL Tube Carton
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INGREDIENTS AND APPEARANCE
ILLUSION LUMINOUS GLOW FOUNDATION (1-26)
avobenzone, homosalate, and octisalate lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 42627-102 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 7.34 g in 100 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 5 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) COCONUT ALKANES (UNII: 1E5KJY107T) DIMETHICONE (UNII: 92RU3N3Y1O) POLYGLYCERYL-4 DIISOSTEARATE/POLYHYDROXYSTEARATE/SEBACATE (UNII: 687U3PEB2Y) TRIBEHENIN (UNII: 8OC9U7TQZ0) DICAPRYLYL ETHER (UNII: 77JZM5516Z) CETYL ALCOHOL (UNII: 936JST6JCN) POLYGLYCERYL-6 POLYRICINOLEATE (UNII: YPM0ZOC2HR) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) ETHYLHEXYL PALMITATE (UNII: 2865993309) GLYCERIN (UNII: PDC6A3C0OX) OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T) SODIUM CHLORIDE (UNII: 451W47IQ8X) SORBITAN MONOOLEATE (UNII: 06XEA2VD56) Dimethicone/Polyglycerin-3 Crosspolymer (UNII: 2P2G24V6T9) POLYGLYCERYL-2 ISOSTEARATE (UNII: 7B8OE71MQC) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L) CAPRYLYL GLYCOL (UNII: 00YIU5438U) GLYCERYL BEHENATE/EICOSADIOATE (UNII: 73CJJ317SR) EICOSYL POVIDONE (UNII: XQQ9MKE2BJ) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) COCOYL CAPRYLOCAPRATE (UNII: 8D9H4QU99H) DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5) ALUMINUM DIMYRISTATE (UNII: J2KA067N9O) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) DISODIUM STEAROYL GLUTAMATE (UNII: 45ASM2L11M) SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) DIPROPYLENE GLYCOL (UNII: E107L85C40) SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR) HYALURONATE SODIUM (UNII: YSE9PPT4TH) TOCOPHEROL (UNII: R0ZB2556P8) HEXYLENE GLYCOL (UNII: KEH0A3F75J) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) SODIUM BENZOATE (UNII: OJ245FE5EU) PHENOXYETHANOL (UNII: HIE492ZZ3T) METHYL SALICYLATE (UNII: LAV5U5022Y) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) FERRIC OXIDE RED (UNII: 1K09F3G675) FERRIC OXIDE YELLOW (UNII: EX438O2MRT) FERROSOFERRIC OXIDE (UNII: XM0M87F357) Product Characteristics Color BROWN Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 42627-102-01 1 in 1 CARTON 12/01/2024 1 35 mL in 1 TUBE; Type 0: Not a Combination Product 2 NDC: 42627-102-02 1 in 1 CARTON 12/01/2024 2 35 mL in 1 TUBE; Type 0: Not a Combination Product 3 NDC: 42627-102-03 1 in 1 CARTON 12/01/2024 3 35 mL in 1 TUBE; Type 0: Not a Combination Product 4 NDC: 42627-102-04 1 in 1 CARTON 12/01/2024 4 35 mL in 1 TUBE; Type 0: Not a Combination Product 5 NDC: 42627-102-05 1 in 1 CARTON 12/01/2024 5 35 mL in 1 TUBE; Type 0: Not a Combination Product 6 NDC: 42627-102-06 1 in 1 CARTON 12/01/2024 6 35 mL in 1 TUBE; Type 0: Not a Combination Product 7 NDC: 42627-102-07 1 in 1 CARTON 12/01/2024 7 35 mL in 1 TUBE; Type 0: Not a Combination Product 8 NDC: 42627-102-08 1 in 1 CARTON 12/01/2024 8 35 mL in 1 TUBE; Type 0: Not a Combination Product 9 NDC: 42627-102-09 1 in 1 CARTON 12/01/2024 9 35 mL in 1 TUBE; Type 0: Not a Combination Product 10 NDC: 42627-102-10 1 in 1 CARTON 12/01/2024 10 35 mL in 1 TUBE; Type 0: Not a Combination Product 11 NDC: 42627-102-11 1 in 1 CARTON 12/01/2024 11 35 mL in 1 TUBE; Type 0: Not a Combination Product 12 NDC: 42627-102-12 1 in 1 CARTON 12/01/2024 12 35 mL in 1 TUBE; Type 0: Not a Combination Product 13 NDC: 42627-102-13 1 in 1 CARTON 12/01/2024 13 35 mL in 1 TUBE; Type 0: Not a Combination Product 14 NDC: 42627-102-14 1 in 1 CARTON 12/01/2024 14 35 mL in 1 TUBE; Type 0: Not a Combination Product 15 NDC: 42627-102-15 1 in 1 CARTON 12/01/2024 15 35 mL in 1 TUBE; Type 0: Not a Combination Product 16 NDC: 42627-102-16 1 in 1 CARTON 12/01/2024 16 35 mL in 1 TUBE; Type 0: Not a Combination Product 17 NDC: 42627-102-17 1 in 1 CARTON 12/01/2024 17 35 mL in 1 TUBE; Type 0: Not a Combination Product 18 NDC: 42627-102-18 1 in 1 CARTON 12/01/2024 18 35 mL in 1 TUBE; Type 0: Not a Combination Product 19 NDC: 42627-102-19 1 in 1 CARTON 12/01/2024 19 35 mL in 1 TUBE; Type 0: Not a Combination Product 20 NDC: 42627-102-20 1 in 1 CARTON 12/01/2024 20 35 mL in 1 TUBE; Type 0: Not a Combination Product 21 NDC: 42627-102-21 1 in 1 CARTON 12/01/2024 21 35 mL in 1 TUBE; Type 0: Not a Combination Product 22 NDC: 42627-102-22 1 in 1 CARTON 12/01/2024 22 35 mL in 1 TUBE; Type 0: Not a Combination Product 23 NDC: 42627-102-23 1 in 1 CARTON 12/01/2024 23 35 mL in 1 TUBE; Type 0: Not a Combination Product 24 NDC: 42627-102-24 1 in 1 CARTON 12/01/2024 24 35 mL in 1 TUBE; Type 0: Not a Combination Product 25 NDC: 42627-102-25 1 in 1 CARTON 12/01/2024 25 35 mL in 1 TUBE; Type 0: Not a Combination Product 26 NDC: 42627-102-26 1 in 1 CARTON 12/01/2024 26 35 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 12/01/2024 Labeler - Kingdom Animalia, LLC DBA Hourglass Cosmetics (004924553) Establishment Name Address ID/FEI Business Operations MANA PRODUCTS INC. 078870292 MANUFACTURE(42627-102) Establishment Name Address ID/FEI Business Operations MANA PRODUCTS INC. 032870270 MANUFACTURE(42627-102)
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