Drug Facts

Active Ingredients

Avobenzone 3.0%

Octisalate 5.0%

Octocrylene 8.0%

Homosalate 7.0%

Purpose

Sunscreen

Use

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.

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.

Stop use and ask a doctor if :

rash occurs.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Apply liberally 15 minutes before sun exposure.
After 80 minutes of swimming.
Immediately after towel drying.
At least every 2 hours.
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 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. Sun Protection Measures:

Other Information

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

Inactive Ingredients

Isododecane, Dimethicone, Silica, Dimethyl Silylate, Caprylyl Methicone, PEG-10 Dimethicone/Vinyl Dimethicone Crosspolymer, Glycerin, PEG-12 Dimethicone/PPG-20 Crosspolymer, Pongamia Pinnata Seed Extract, Limnanthes Alba (Meadowfoam) Seed Oil, Aloe Barbadensis Leaf Juice Powder, Polyester-7, Neopentyl Glycol Diheptanoate, Phenoxyethanol, Ethylhexylglycerin, Isopropyl Palmitate

Question or comments?

1-888-315-9814

Package Labeling:50ml

Label

Package Labeling:10ml

Label2

E.L.F INVISIBLE SUNSCREEN SPF 35
avobenzone, octisalate, octocrylene, homosalate cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:76354-444
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	30 mg in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	50 mg in 1 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	80 mg in 1 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	70 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
ISODODECANE (UNII: A8289P68Y2)
DIMETHICONE (UNII: 92RU3N3Y1O)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)
GLYCERIN (UNII: PDC6A3C0OX)
PEG-12 DIMETHICONE/PPG-20 CROSSPOLYMER (UNII: 965K72OQXO)
PONGAMIA PINNATA SEED (UNII: C2BRV53B1V)
MEADOWFOAM SEED OIL (UNII: 412ZHA4T4Y)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
POLYESTER-7 (UNII: 0841698D2F)
NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:76354-444-01	1 in 1 CARTON	02/15/2023
1		50 mL in 1 TUBE; Type 0: Not a Combination Product
2	NDC:76354-444-02	1 in 1 CARTON	02/15/2023
2		10 mL in 1 TUBE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M020	02/15/2023

Labeler - e.l.f. Cosmetics, Inc (093902816)

e.l.f Invisible Sunscreen SPF 35