Label: HOMOSALATE 10 AVOBENZONE 3% OCTOCRYLENE 6%- spf 45 face lotion
- NDC Code(s): 87170-003-01, 87170-003-02
- Packager: S&C Hampton Sun LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 26, 2026
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- Official Label (Printer Friendly)
- Active Ingredients
- Purpous
- Uses
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Directions
• apply liberally and spread evenly by hand 15 minutes before sun exposure • reapply: • after 80 minutes of swimming or sweating • immediately after towel drying • at least every 2 hours
• Sun Protection Measures. Spending tme 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 a long-sleeve shirt, pants, hats, and sunglasses.
• children under 6 months: Ask a doctor. - Warning
- Keep out of reach children.
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Inactive Ingredients
ALUMINUM STARCH OCTENYLSUCCINATE
AMINOMETHYLPROPANOL
ARACHIDIC ACID
BENZYL ALCOHOL
BUTYLOCTYL SALICYLATE
CARBOMER
CELLULOSE GUM
DIMETHICONE
ETHYLHEXYLGLYCERIN
GLYCERIN
LAURIC ACID
MYRISTIC ACID
PALMITIC ACID
PHENOXYETHANOL
SODIUM HYALURONATE
SODIUM PHYTATE
SODIUM POLYACRYLATE
SORBITAN ISOSTEARATE
SORBITOL
STEARIC ACID
VP/EICOSENE COPOLYMER
WATER
OXIDES - PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
HOMOSALATE 10 AVOBENZONE 3% OCTOCRYLENE 6%
spf 45 face lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:87170-003 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 6 g in 100 mL HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 10 g in 100 mL AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 3 g in 100 mL Inactive Ingredients Ingredient Name Strength ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294) AMINOMETHYLPROPANOL (UNII: LU49E6626Q) ARACHIDIC ACID (UNII: PQB8MJD4RB) BENZYL ALCOHOL (UNII: LKG8494WBH) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) CARBOMER (UNII: 0A5MM307FC) CELLULOSE GUM (UNII: K679OBS311) DIMETHICONE (UNII: 92RU3N3Y1O) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) GLYCERIN (UNII: PDC6A3C0OX) LAURIC ACID (UNII: 1160N9NU9U) MYRISTIC ACID (UNII: 0I3V7S25AW) PALMITIC ACID (UNII: 2V16EO95H1) PHENOXYETHANOL (UNII: HIE492ZZ3T) SODIUM HYALURONATE (UNII: YSE9PPT4TH) SODIUM PHYTATE (UNII: 88496G1ERL) SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L) SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4) SORBITOL (UNII: 506T60A25R) STEARIC ACID (UNII: 4ELV7Z65AP) VINYLPYRROLIDONE/EICOSENE COPOLYMER (UNII: 035MV9S1C3) WATER (UNII: 059QF0KO0R) BROWN IRON OXIDE (UNII: 1N032N7MFO) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:87170-003-02 59 mL in 1 TUBE; Type 0: Not a Combination Product 01/15/2024 2 NDC:87170-003-01 20 mL in 1 TUBE; Type 0: Not a Combination Product 01/15/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 01/15/2024 Labeler - S&C Hampton Sun LLC (031880374) Registrant - Inspec Solutions LLC (081030372) Establishment Name Address ID/FEI Business Operations Inspec Solutions LLC 081030372 manufacture(87170-003)
