Label: SUN BUM SUNSCREEN LIP BALM BROAD SPECTRUM SPF 30 KIWI- avobenzone, homosalate, octisalate, octocrylene stick
- NDC Code(s): 69039-819-01
- Packager: Sun Bum, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated August 21, 2025
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- Active Ingredients
- Purpose
- Uses
- Warnings
- Warnings
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Directions
• apply liberally 15 minutes before sun exposure
• reapply: • after 80 minutes of swimming or sweating • immediately after towel drying • at least every 2 hours
• children under 6 months of age: ask a doctor
• 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
- Directions
- Other Information
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Inactive Ingredients
aloe barbadensis leaf extract, argania spinosa kernel oil, bisabolol, camellia sinensis leaf extract, caprylic/capric triglyceride, calendula officinalis flower extract, cetyl alcohol, citrus grandis fruit extract, citrus limon peel extract, cucumis sativus (cucumber) fruit extract, diisobutyl adipate, equisetum arvense extract, ethylhexyl palmitate, fragrance, ginkgo biloba leaf extract, hydrogenated ethylhexyl olivate, hydrogenated olive oil unsaponifiables, isostearyl linoleate, macrocystis pyrifera extract, mineral oil, ozokerite, panax ginseng root extract, PEG-8, polysorbate 80, propylene glycol, punica granatum extract, rosmarinus officinalis extract, saccharin, salix alba (willow) bark extract, salvia officinalis (sage) extract, silica, theobroma cacao seed butter, tocopheryl acetate, tocopheryl linoleate/oleate, water
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INGREDIENTS AND APPEARANCE
SUN BUM SUNSCREEN LIP BALM BROAD SPECTRUM SPF 30 KIWI
avobenzone, homosalate, octisalate, octocrylene stickProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69039-819 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 g HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 100 mg in 1 g OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 50 mg in 1 g OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 80 mg in 1 g Inactive Ingredients Ingredient Name Strength .ALPHA.-TOCOPHEROL LINOLEATE, D- (UNII: G0N132Q0ED) WATER (UNII: 059QF0KO0R) HYDROGENATED OLIVE OIL UNSAPONIFIABLES (UNII: B8MIX97W95) ISOSTEARYL LINOLEATE (UNII: 4778M3HR0N) EQUISETUM ARVENSE WHOLE (UNII: 73DM367W4P) ETHYLHEXYL PALMITATE (UNII: 2865993309) BISABOLOL (UNII: 24WE03BX2T) CAMELLIA SINENSIS LEAF (UNII: W2ZU1RY8B0) CAPRYLIC/CAPRIC TRIGLYCERIDE (UNII: C9H2L21V7U) CETYL ALCOHOL (UNII: 936JST6JCN) GRAPEFRUIT (UNII: O82C39RR8C) LEMON PEEL (UNII: 72O054U628) DIISOBUTYL ADIPATE (UNII: 8OPY05ZY7S) PANAX GINSENG ROOT (UNII: CUQ3A77YXI) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) ARGANIA SPINOSA KERNEL OIL (UNII: 4V59G5UW9X) GINKGO BILOBA LEAF (UNII: 19FUJ2C58T) PUNICA GRANATUM WHOLE (UNII: O2ZTS50U5E) SACCHARIN (UNII: FST467XS7D) SILICA (UNII: ETJ7Z6XBU4) ALOE BARBADENSIS LEAF (UNII: ZY81Z83H0X) CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD) CUCUMIS SATIVUS (CUCUMBER) FRUIT (UNII: YY7C30VXJT) ROSMARINUS OFFICINALIS WHOLE (UNII: EA3289138M) WILLOW BARK (UNII: S883J9JDYX) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) THEOBROMA CACAO (COCOA) SEED BUTTER (UNII: 512OYT1CRR) MACROCYSTIS PYRIFERA (KELP) (UNII: K31S3OG5C4) CERESIN (UNII: Q1LS2UJO3A) PEG-8 (UNII: B697894SGQ) HYDROGENATED ETHYLHEXYL OLIVATE (UNII: JBH5K4WD8L) MINERAL OIL (UNII: T5L8T28FGP) POLYSORBATE 80 (UNII: 6OZP39ZG8H) SAGE (UNII: 065C5D077J) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69039-819-01 4.25 g in 1 TUBE, WITH APPLICATOR; Type 0: Not a Combination Product 08/01/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 08/01/2024 Labeler - Sun Bum, LLC (028642574)
