UNSEEN SUNSCREEN BROAD SPECTRUM SPF 40- avobenzone, homosalate, octinoxate, octisalate cream 
Supergoop, LLC

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.

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Unseen Sunscreen Broad Spectrum SPF 40

Active Ingredients        Purpose

Avobenzone 3%          Sunscreen

Homosalate 8%          Sunscreen

Octocrylene 4%         Sunscreen

Octisalate 5%             Sunscreen

Uses

  • Helps prevent sunburn
  • If used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun

Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

Stop use and ask a doctor if rash occurs

Warnings

For external use only

Do not use on damaged or broken skin

Directions

  • apply generously and evenly 15 minutes before sun exposure
  • reapply:

after 40 minutes of swimming or sweating

immediately after towel drying

at least every 2 hours

  • 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
  • Children under 6 months: ask a doctor

Inactive Ingredients

Isododecane, Dimethicone Crosspolymer, Dimethicone/Bis-Isobutyl PPG-20 Crosspolymer, Polymethylsilsesquioxane, Isohexadecane, Dicrapylyl Carbonate, Meadowfoam Estolide, Caprylic/Capric Triglyceride, Polyester-7, Neopentyl Glycol Diheptanoate, Lithothamnion Calcareum Extract,Butyrospermum Parkii (Shea) Butter, Jojoba Esters, Mannitol, Boswellia Serrata Resin Extract, Lecithin, Microcrystalline Cellulose, Diatomaceous Earth, Zinc Sulfate, Silica, Tocopherol

Supergoop

Unseen Sunscreen

Broad Spectrum SPF 40

Water and sweat resistant (40 minutes)

1.7 fl oz/ 50 ml

CartonTube

UNSEEN SUNSCREEN BROAD SPECTRUM SPF 40 
avobenzone, homosalate, octinoxate, octisalate cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75936-164
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE3 g  in 100 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE8 g  in 100 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE4 g  in 100 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE5 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
ISODODECANE (UNII: A8289P68Y2)  
DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE) (UNII: UF7620L1W6)  
DIMETHICONE/BIS-ISOBUTYL PPG-20 CROSSPOLYMER (UNII: O4I3UFO6ZF)  
ISOHEXADECANE (UNII: 918X1OUF1E)  
DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)  
POLYESTER-7 (UNII: 0841698D2F)  
NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)  
POLYMETHYLSILSESQUIOXANE (11 MICRONS) (UNII: Z570VEV8XK)  
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
PHYMATOLITHON CALCAREUM (UNII: 6J1M3WA0ZK)  
SHEA BUTTER (UNII: K49155WL9Y)  
DIETHYLHEXYL SYRINGYLIDENEMALONATE (UNII: 3V5U97P248)  
MANNITOL (UNII: 3OWL53L36A)  
INDIAN FRANKINCENSE (UNII: 4PW41QCO2M)  
LECITHIN, SUNFLOWER (UNII: 834K0WOS5G)  
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
DIATOMACEOUS EARTH (UNII: 2RF6EJ0M85)  
ZINC SULFATE (UNII: 89DS0H96TB)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
TOCOPHEROL (UNII: R0ZB2556P8)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:75936-164-021 in 1 CARTON10/12/2017
1NDC:75936-164-0150 mL in 1 PACKAGE; Type 0: Not a Combination Product
2NDC:75936-164-0615 mL in 1 TUBE; Type 0: Not a Combination Product10/12/2017
3NDC:75936-164-0310 mL in 1 PACKAGE; Type 0: Not a Combination Product10/12/2017
4NDC:75936-164-045 mL in 1 PACKAGE; Type 0: Not a Combination Product10/12/2017
5NDC:75936-164-051.5 mL in 1 PACKAGE; Type 0: Not a Combination Product10/12/2017
6NDC:75936-164-0730 mL in 1 TUBE; Type 0: Not a Combination Product08/17/2020
7NDC:75936-164-0820 mL in 1 CARTON; Type 0: Not a Combination Product02/15/2021
8NDC:75936-164-0973.9 mL in 1 TUBE; Type 0: Not a Combination Product10/27/2017
9NDC:75936-164-111 in 1 CARTON10/10/2017
9NDC:75936-164-1050 mL in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35210/10/2017
Labeler - Supergoop, LLC (117061743)

Revised: 10/2022
 
Supergoop, LLC