LIP SCREEN SHEER SPF 30- octocrylene, avobenzone, homosalate, octisalate lipstick

Lip Screen Sheer SPF 30 by

Drug Labeling and Warnings

Lip Screen Sheer SPF 30 by is a Otc medication manufactured, distributed, or labeled by Supergoop LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Uses

Help 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

Warnings

Do not use on damaged or broken skin.

Warnings

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

Warnings

Stop use and ask a doctor if rash occurs.

Warnings

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

Directions

• Apply generously and evenly 15 minutes before sun exposure
• Reapply at least every 2 hours
• use a water-resistant sunscreen if swimming or sweating

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 10am-2pm
• Wear long-sleeved shirts, pants, hats, and sunglasses
• Children under 6 months: Ask a doctor

Inactive Ingredients

Octoyldodecanol, C12-15 Alkyl Benzoate, Ricinus Communis (Castor) Seed Oil, Diisostearyl Malate, Flavor, Dibutyl Lauroyl Glutamide, Phenethyl Benzoate, Dibutyl Ethylhexanoyl Glutamide, Silica Silylate, Brassica Campestris/Aleurites Fordi Oil Crosspolymer, Octyldodecyl Neopentanoate, Saccharin, Tocopherol, Euterpe Oleracea Fruit Oil

Other Information

Protect the product in this container from excessive heat and direct sun

Questions or comments?

Contact our Sun Specialist

877-564-7330

PDP

Lip Screen Sheer SPF 30

Unseen shade

INGREDIENTS AND APPEARANCE

LIP SCREEN SHEER SPF 30 
octocrylene, avobenzone, homosalate, octisalate lipstick

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75936-602
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	3 mg  in 100 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	9 mg  in 100 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	5 mg  in 100 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	9 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W)
OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T)
SACCHARIN (UNII: FST467XS7D)
EUTERPE OLERACEA WHOLE (UNII: Y57H6218HP)
TOCOPHEROL (UNII: R0ZB2556P8)
OCTYLDODECANOL (UNII: 461N1O614Y)
BRASSICA RAPA VAR. RAPA OIL (UNII: N4G8379626)
DRYOBALANOPS AROMATICA WHOLE (UNII: 34303GFW6A)
DIBUTYL LAUROYL GLUTAMIDE (UNII: 3V7K3IA58X)
DIBUTYL ETHYLHEXANOYL GLUTAMIDE (UNII: 0IAF2L30VS)
DIISOSTEARYL MALATE (UNII: QBS8A3XZGQ)
PHENETHYL BENZOATE (UNII: 0C143929GK)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
RICINUS COMMUNIS SEED (UNII: 7EK4SFN1TX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75936-602-02	1 in 1 CARTON	03/25/2022
1	NDC: 75936-602-01	3.5 mL in 1 TUBE, WITH APPLICATOR; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part352	03/25/2022

Labeler - Supergoop LLC (117061743)