Label: FLORIDA SQUEEZE SPF 15- avobenzone, homosalate, octisalate spray
FLORIDA SQUEEZE SPF 8- avobenzone, homosalate, octisalate spray
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Contains inactivated NDC Code(s)
NDC Code(s): 73440-2800-1, 73440-2801-1 - Packager: Cross Brands Contract Filling
- 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 August 5, 2022
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- Official Label (Printer Friendly)
- Florida Squeeze Spray SPF 15
- Florida Squeeze Spray SPF 8
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INGREDIENTS AND APPEARANCE
FLORIDA SQUEEZE SPF 15
avobenzone, homosalate, octisalate sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73440-2801 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 5.1 g in 170 g OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 8.5 g in 170 g HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 12.75 g in 170 g Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) 129.71 g in 170 g Product Characteristics Color yellow (Clear to semi-opaque liquid) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73440-2801-1 170 g in 1 CAN; Type 0: Not a Combination Product 07/01/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 07/01/2021 FLORIDA SQUEEZE SPF 8
avobenzone, homosalate, octisalate sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73440-2800 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 5.1 g in 170 g HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 12.75 g in 170 g OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 8.5 g in 170 g Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) 129.71 g in 170 g Product Characteristics Color yellow (Clear to semi-opaque liquid) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73440-2800-1 170 g in 1 CAN; Type 0: Not a Combination Product 07/01/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 07/01/2021 Labeler - Cross Brands Contract Filling (117871824) Establishment Name Address ID/FEI Business Operations Cross Brands Contract Filling 117871824 pack(73440-2801, 73440-2800) , label(73440-2801, 73440-2800) , manufacture(73440-2801, 73440-2800)
