Label: SOLIMO SPORT SPF 30 SUNSCREEN- avobenzone, homosalate, octocrylene lotion
- NDC Code(s): 72288-203-40, 72288-203-41
- Packager: Amazon.com Services LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated October 6, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredients
- Purpose
- Uses
- Warnings
- DO NOT USE
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
-
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 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
- Other Information
-
Inactive ingredients
water, cetearyl alcohol, stearyl alcohol, glycerin, acrylates/C12-22 alkyl methacrylate copolymer, cetyl alcohol, carbomer, ceteth-10 phosphate, dicetyl phosphate, coco-glucoside, xanthan gum, disodium EDTA, methyl dihydrobietate, lauryl PEG-8 dimethicone, phenylisopropyl dimethicone, polyglecryl-3 stearate/isostearate/dimer dilinoleate crosspolymer, sodium ascorbyl phosphate, tocopheryl acetate, aloe barbadensis leaf juice, phenoxyethanol, triethanolamine, propylene glycol, hydroxyacetophenone
- Questions or comments?
- Solimo Sport SPF 30 Sunscreen Lotion
-
INGREDIENTS AND APPEARANCE
SOLIMO SPORT SPF 30 SUNSCREEN
avobenzone, homosalate, octocrylene lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72288-203 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 18 mg in 1 mL HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 70 mg in 1 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 50 mg in 1 mL Inactive Ingredients Ingredient Name Strength LAURYL PEG/PPG-18/18 METHICONE (UNII: ZJ5S27D9NX) STEARIC ACID (UNII: 4ELV7Z65AP) .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) WATER (UNII: 059QF0KO0R) ISOSTEARIC ACID (UNII: X33R8U0062) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) DIHEXADECYL PHOSPHATE (UNII: 2V6E5WN99N) CETYL ALCOHOL (UNII: 936JST6JCN) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) BUTYL ACRYLATE/C16-C20 ALKYL METHACRYLATE/METHACRYLIC ACID/METHYL METHACRYLATE COPOLYMER (UNII: 7K68DGG29P) GLYCERIN (UNII: PDC6A3C0OX) METHYL DIHYDROABIETATE (UNII: 7666FJ0J9F) POLYGLYCERIN-3 (UNII: 4A0NCJ6RD6) DILINOLEIC ACID (UNII: 5RP695IQQ3) CETETH-10 PHOSPHATE (UNII: 4E05O5N49G) POLY(LAURYLGLUCOSIDE)-7 (UNII: VB00RDE21R) PHENOXYETHANOL (UNII: HIE492ZZ3T) ALOE VERA LEAF (UNII: ZY81Z83H0X) SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR) HYDROXYACETOPHENONE (UNII: G1L3HT4CMH) TROLAMINE (UNII: 9O3K93S3TK) CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC) XANTHAN GUM (UNII: TTV12P4NEE) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72288-203-40 308 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/02/2018 2 NDC:72288-203-41 616 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/02/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 05/02/2018 Labeler - Amazon.com Services LLC (128990418)
