LIP SCREEN BROAD SPECTRUM SPF 40- avobenzone, homosalate, octisalate, octocrylene liquid 
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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Lip Screen Broad Spectrum SPF 40

Avobenzone 3% Sunscreen

Homosalate 5% Sunscreen

Octisalate 5% Sunscreen

Octocrylene 10% 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

When using this product keep out of eyes. Rinse with water to remove

Directions

Apply generously and evenly 15 minutes before sun exposure
Use a water-resistant sunscreen if swimming or sweating
Reapply 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 your time in the sun, especially from 10
a.m. – 2 p.m. • wear long-sleeved shirts, pants, hats, and sunglasses •
Children under 6 months of age: ask a doctor.

Inactive Ingredients

Hydrogenated Polyisobutene, Diisostearyl Malate, Caprylic/Capric Triglyceride, Butyloctyl Salicylate, C12-15 Alkyl Benzoate, Polyurethane-79, Polyester-7, Butyrospermum Parkii (Shea) Butter, Cocos Nucifera (Coconut) Oil, Isopropyl Palmitate , Sesamum Inidicum (Sesame) Seed Oil, Neopentyl Glycol Diheptanoate, Diethylhexyl Syringlidenemalonate, Caprylyl Glycol, Glycine Soja (Soybean) Oil, Tocopherol, 2-Methylbutyric Acid, Barosma Betulina Leaf Oil, Benzaldehyde, Dimethylhydroxy Furanone, Trans-2-Hexenal, Helianthus Annuus (Sunflower) Seed Oil, Ethyl Acetate, Stevioside, Gamma-Undecalactone, Vanillin, Vitis Vinifera (Grape) Seed Extract, Laminaria Ochroleuca Extract, Citric Acid

Lip Screen

SPF 40

Broad Spectrum SPF 40

0.34 fl. oz. / 10 ml.

CartonTube

LIP SCREEN BROAD SPECTRUM SPF 40 
avobenzone, homosalate, octisalate, octocrylene liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75936-257
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE3 g  in 100 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE10 g  in 100 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE5 g  in 100 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE5 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
ETHYL ACETATE (UNII: 76845O8NMZ)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
POLYESTER-7 (UNII: 0841698D2F)  
TOCOPHEROL (UNII: R0ZB2556P8)  
DIMETHYLHYDROXY FURANONE (UNII: 20PI8YZP7A)  
2-HEXENAL, (2E)- (UNII: 69JX3AIR1I)  
DIETHYLHEXYL SYRINGYLIDENEMALONATE (UNII: 3V5U97P248)  
LAMINARIA OCHROLEUCA (UNII: 4R2124HE76)  
AGATHOSMA BETULINA LEAF OIL (UNII: KOS935A04V)  
VANILLIN (UNII: CHI530446X)  
2-METHYLBUTYRIC ACID (UNII: PX7ZNN5GXK)  
SESAME OIL (UNII: QX10HYY4QV)  
.GAMMA.-UNDECALACTONE (UNII: QB1T0AG2YL)  
DIISOSTEARYL MALATE (UNII: QBS8A3XZGQ)  
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)  
HYDROGENATED POLYBUTENE (1300 MW) (UNII: 7D1YQ9Y5EZ)  
STEVIOSIDE (UNII: 0YON5MXJ9P)  
VITIS VINIFERA SEED (UNII: C34U15ICXA)  
SHEA BUTTER (UNII: K49155WL9Y)  
COCONUT OIL (UNII: Q9L0O73W7L)  
ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)  
NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)  
SOYBEAN OIL (UNII: 241ATL177A)  
BENZALDEHYDE (UNII: TA269SD04T)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:75936-257-0110 mL in 1 TUBE; Type 0: Not a Combination Product04/22/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35204/22/2020
Labeler - Supergoop, LLC (117061743)

Revised: 7/2023
Document Id: 00383aa5-1310-f75f-e063-6294a90ab305
Set id: a3e5819a-5132-9760-e053-2a95a90a058b
Version: 6
Effective Time: 20230711
 
Supergoop, LLC