Label: NATURIUM PHYTO-GLOW LIP BALM SPF 45-OASIS- avobenzone, homosalate, octisalate cream
NATURIUM PHYTO-GLOW LIP BALM SPF 45-ESCAPE- avobenzone, homosalate, octisalate cream
NATURIUM PHYTO-GLOW LIP BALM SPF 45-PARADISE- avobenzone, homosalate, octisalate cream
NATURIUM PHYTO-GLOW LIP BALM SPF 45-GETAWAY- avobenzone, homosalate, octisalate cream
- NDC Code(s): 76354-136-01, 76354-137-01, 76354-138-01, 76354-139-01
- Packager: e.l.f. Cosmetics, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated June 9, 2025
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- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredients
- Uses
- Warnings
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Directions
- Apply liberally 15 minutes before sun exposure. Reapply at least every 2 hours.
- Use 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 Board Spectrum SPF value of 15 or higher and other sun protection measures including: limit time in 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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InactiveIngredients
Phytosteryl/Isostearyl/Cetyl/Stearyl/Behenyl Dimer Dilinoleate, Diisostearyl Malate, Polybutene, Hydrogenated Polyisobutene, Aroma/Flavor, Polyglyceryl-2 Diisostearate, Butyrospermum Parkii (Shea) Butter, Cera Microcristallina/Microcrystalline Wax/Cire Microcristalline, C12-15 Alkyl Benzoate, Ethylhexyl Methoxycrylene, Synthetic Wax, Mica, Squalane, Theobroma Grandiflorum Seed Butter, Siraitia Grosvenorii Fruit Extract, Tocopherol, Citric Acid, BHT, Carvone, Cinnamal, Eugenol, Limonene, Menthol, Methyl Salicylate, Vanillin.
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INGREDIENTS AND APPEARANCE
NATURIUM PHYTO-GLOW LIP BALM SPF 45-OASIS
avobenzone, homosalate, octisalate creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76354-137 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 30 mg in 1 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 50 mg in 1 mL Inactive Ingredients Ingredient Name Strength CINNAMAL (UNII: SR60A3XG0F) RED 6 (UNII: 481744AI4O) RICINUS COMMUNIS (CASTOR) SEED OIL (UNII: D5340Y2I9G) YELLOW 5 (UNII: I753WB2F1M) POLYGLYCERYL-2 DIISOSTEARATE (UNII: DG195GP57P) SIRAITIA GROSVENORII FRUIT (UNII: NOU2FB51TW) CITRIC ACID (UNII: 2968PHW8QP) MICROCRYSTALLINE WAX (UNII: XOF597Q3KY) BHT (UNII: 1P9D0Z171K) LIMONENE, (+)- (UNII: GFD7C86Q1W) METHYL SALICYLATE (UNII: LAV5U5022Y) TOCOPHEROL (UNII: R0ZB2556P8) C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ) THEOBROMA GRANDIFLORUM SEED BUTTER (UNII: I711F13FXM) PHYTOSTERYL/ISOSTEARYL/CETYL/STEARYL/BEHENYL DIMER DILINOLEATE (UNII: 8N725H4EFN) EUGENOL (UNII: 3T8H1794QW) VANILLIN (UNII: CHI530446X) POLYBUTENE (1400 MW) (UNII: 1NA5AO9GH7) CARVONE (UNII: 75GK9XIA8I) MICA (UNII: V8A1AW0880) HYDROGENATED POLYISOBUTENE (450 MW) (UNII: 7YR4ZFS62E) SYNTHETIC WAX (1200 MW) (UNII: Q3Z4BCH099) ETHYLHEXYL METHOXYCRYLENE (UNII: S3KFG6Q5X8) BUTYROSPERMUM PARKII (SHEA) BUTTER (UNII: K49155WL9Y) SQUALANE (UNII: GW89575KF9) FLAVOR SPICE MINT N&A110589 (UNII: KG6KU384XW) MENTHOL (UNII: L7T10EIP3A) DIISOSTEARYL MALATE (UNII: QBS8A3XZGQ) BLUE 1 LAKE (UNII: J9EQA3S2JM) RED 7 (UNII: ECW0LZ41X8) ISOPROPYL TITANIUM TRIISOSTEARATE (UNII: 949E3KBJ1I) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) FERROSOFERRIC OXIDE (UNII: XM0M87F357) FERRIC OXIDE YELLOW (UNII: EX438O2MRT) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76354-137-01 1 in 1 CARTON 06/09/2025 1 10 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 06/09/2025 NATURIUM PHYTO-GLOW LIP BALM SPF 45-ESCAPE
avobenzone, homosalate, octisalate creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76354-139 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 30 mg in 1 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 50 mg in 1 mL Inactive Ingredients Ingredient Name Strength CINNAMAL (UNII: SR60A3XG0F) RED 6 (UNII: 481744AI4O) RICINUS COMMUNIS (CASTOR) SEED OIL (UNII: D5340Y2I9G) YELLOW 5 (UNII: I753WB2F1M) POLYGLYCERYL-2 DIISOSTEARATE (UNII: DG195GP57P) SIRAITIA GROSVENORII FRUIT (UNII: NOU2FB51TW) CITRIC ACID (UNII: 2968PHW8QP) MICROCRYSTALLINE WAX (UNII: XOF597Q3KY) BHT (UNII: 1P9D0Z171K) LIMONENE, (+)- (UNII: GFD7C86Q1W) METHYL SALICYLATE (UNII: LAV5U5022Y) TOCOPHEROL (UNII: R0ZB2556P8) C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ) THEOBROMA GRANDIFLORUM SEED BUTTER (UNII: I711F13FXM) PHYTOSTERYL/ISOSTEARYL/CETYL/STEARYL/BEHENYL DIMER DILINOLEATE (UNII: 8N725H4EFN) EUGENOL (UNII: 3T8H1794QW) VANILLIN (UNII: CHI530446X) POLYBUTENE (1400 MW) (UNII: 1NA5AO9GH7) CARVONE (UNII: 75GK9XIA8I) MICA (UNII: V8A1AW0880) HYDROGENATED POLYISOBUTENE (450 MW) (UNII: 7YR4ZFS62E) SYNTHETIC WAX (1200 MW) (UNII: Q3Z4BCH099) ETHYLHEXYL METHOXYCRYLENE (UNII: S3KFG6Q5X8) BUTYROSPERMUM PARKII (SHEA) BUTTER (UNII: K49155WL9Y) SQUALANE (UNII: GW89575KF9) FLAVOR SPICE MINT N&A110589 (UNII: KG6KU384XW) MENTHOL (UNII: L7T10EIP3A) DIISOSTEARYL MALATE (UNII: QBS8A3XZGQ) BLUE 1 LAKE (UNII: J9EQA3S2JM) RED 7 (UNII: ECW0LZ41X8) ISOPROPYL TITANIUM TRIISOSTEARATE (UNII: 949E3KBJ1I) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) FERROSOFERRIC OXIDE (UNII: XM0M87F357) FERRIC OXIDE YELLOW (UNII: EX438O2MRT) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76354-139-01 1 in 1 CARTON 06/09/2025 1 10 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 06/09/2025 NATURIUM PHYTO-GLOW LIP BALM SPF 45-PARADISE
avobenzone, homosalate, octisalate creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76354-138 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 30 mg in 1 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 50 mg in 1 mL Inactive Ingredients Ingredient Name Strength CINNAMAL (UNII: SR60A3XG0F) RED 6 (UNII: 481744AI4O) RICINUS COMMUNIS (CASTOR) SEED OIL (UNII: D5340Y2I9G) YELLOW 5 (UNII: I753WB2F1M) POLYGLYCERYL-2 DIISOSTEARATE (UNII: DG195GP57P) SIRAITIA GROSVENORII FRUIT (UNII: NOU2FB51TW) CITRIC ACID (UNII: 2968PHW8QP) MICROCRYSTALLINE WAX (UNII: XOF597Q3KY) BHT (UNII: 1P9D0Z171K) LIMONENE, (+)- (UNII: GFD7C86Q1W) METHYL SALICYLATE (UNII: LAV5U5022Y) TOCOPHEROL (UNII: R0ZB2556P8) C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ) THEOBROMA GRANDIFLORUM SEED BUTTER (UNII: I711F13FXM) PHYTOSTERYL/ISOSTEARYL/CETYL/STEARYL/BEHENYL DIMER DILINOLEATE (UNII: 8N725H4EFN) EUGENOL (UNII: 3T8H1794QW) VANILLIN (UNII: CHI530446X) POLYBUTENE (1400 MW) (UNII: 1NA5AO9GH7) CARVONE (UNII: 75GK9XIA8I) MICA (UNII: V8A1AW0880) HYDROGENATED POLYISOBUTENE (450 MW) (UNII: 7YR4ZFS62E) SYNTHETIC WAX (1200 MW) (UNII: Q3Z4BCH099) ETHYLHEXYL METHOXYCRYLENE (UNII: S3KFG6Q5X8) BUTYROSPERMUM PARKII (SHEA) BUTTER (UNII: K49155WL9Y) SQUALANE (UNII: GW89575KF9) FLAVOR SPICE MINT N&A110589 (UNII: KG6KU384XW) MENTHOL (UNII: L7T10EIP3A) DIISOSTEARYL MALATE (UNII: QBS8A3XZGQ) BLUE 1 LAKE (UNII: J9EQA3S2JM) RED 7 (UNII: ECW0LZ41X8) ISOPROPYL TITANIUM TRIISOSTEARATE (UNII: 949E3KBJ1I) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) FERROSOFERRIC OXIDE (UNII: XM0M87F357) FERRIC OXIDE YELLOW (UNII: EX438O2MRT) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76354-138-01 1 in 1 CARTON 06/09/2025 1 10 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 06/09/2025 NATURIUM PHYTO-GLOW LIP BALM SPF 45-GETAWAY
avobenzone, homosalate, octisalate creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76354-136 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 30 mg in 1 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 50 mg in 1 mL Inactive Ingredients Ingredient Name Strength RED 6 (UNII: 481744AI4O) RICINUS COMMUNIS (CASTOR) SEED OIL (UNII: D5340Y2I9G) BHT (UNII: 1P9D0Z171K) YELLOW 5 (UNII: I753WB2F1M) POLYGLYCERYL-2 DIISOSTEARATE (UNII: DG195GP57P) SIRAITIA GROSVENORII FRUIT (UNII: NOU2FB51TW) CITRIC ACID (UNII: 2968PHW8QP) MICROCRYSTALLINE WAX (UNII: XOF597Q3KY) LIMONENE, (+)- (UNII: GFD7C86Q1W) METHYL SALICYLATE (UNII: LAV5U5022Y) TOCOPHEROL (UNII: R0ZB2556P8) C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ) THEOBROMA GRANDIFLORUM SEED BUTTER (UNII: I711F13FXM) PHYTOSTERYL/ISOSTEARYL/CETYL/STEARYL/BEHENYL DIMER DILINOLEATE (UNII: 8N725H4EFN) EUGENOL (UNII: 3T8H1794QW) VANILLIN (UNII: CHI530446X) POLYBUTENE (1400 MW) (UNII: 1NA5AO9GH7) CARVONE (UNII: 75GK9XIA8I) MICA (UNII: V8A1AW0880) HYDROGENATED POLYISOBUTENE (450 MW) (UNII: 7YR4ZFS62E) SYNTHETIC WAX (1200 MW) (UNII: Q3Z4BCH099) ETHYLHEXYL METHOXYCRYLENE (UNII: S3KFG6Q5X8) BUTYROSPERMUM PARKII (SHEA) BUTTER (UNII: K49155WL9Y) SQUALANE (UNII: GW89575KF9) FLAVOR SPICE MINT N&A110589 (UNII: KG6KU384XW) MENTHOL (UNII: L7T10EIP3A) DIISOSTEARYL MALATE (UNII: QBS8A3XZGQ) CINNAMAL (UNII: SR60A3XG0F) BLUE 1 LAKE (UNII: J9EQA3S2JM) FERRIC OXIDE YELLOW (UNII: EX438O2MRT) RED 7 (UNII: ECW0LZ41X8) ISOPROPYL TITANIUM TRIISOSTEARATE (UNII: 949E3KBJ1I) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) FERROSOFERRIC OXIDE (UNII: XM0M87F357) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76354-136-01 1 in 1 CARTON 06/09/2025 1 10 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 06/09/2025 Labeler - e.l.f. Cosmetics, Inc. (093902816)




