Drug Facts

Active Ingredients

Avobenzone 3%

Homosalate 10%

Octisalate 5%

Octocrylene 3%

Purpose

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.

Warnings

Avoid contact with eyes.
For external use only.

Do not use

on damaged or broken skin. 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
Use a water resistant sunscreen if swimming or sweating
Reapply at least every 2 hours
Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease risk, regularly use a sunscreen SPF value of 15 or higher and other sun protection measures including: Sun Protection Measures.
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

Other information

Protect the product in this container from excessive heat and direct sunlight.
You may report a serious adverse event from use of this product to: team@kravebeauty.com

Inactive Ingredients

Water (Aqua), Propanediol, Pentylene Glycol, Sodium Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Bisabolol, Ethylhexyl Methoxycrylene, Hydroxyacetophenone, Beta Vulgaris (Beet) Root Extract, Isohexadecane, Polysorbate 80, Hyaluronic Acid, Tocopheryl Acetate, Caprylyl Glycol, Eugenia Caryophyllus Bud Extract, Solidago Virgaurea Extract, Salix Alba (Willow) Bark Extract, Trisodium Ethylenediamine Disuccinate, 1,2-Hexanediol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Xanthan Gum, Citric Acid, Sodium Hydroxide

Package Labeling:

Outer Package Inner Package

BEET THE SUN LIGHTWEIGHT SUNSCREEN BROAD SPECTRUM SPF 40 PA
avobenzone, homosalate, octisalate, octocrylene lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:83493-150
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
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	100 mg in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	50 mg in 1 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	30 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
PROPANEDIOL (UNII: 5965N8W85T)
PENTYLENE GLYCOL (UNII: 50C1307PZG)
LEVOMENOL (UNII: 24WE03BX2T)
ETHYLHEXYL METHOXYCRYLENE (UNII: S3KFG6Q5X8)
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
BEET (UNII: N487KM8COK)
ISOHEXADECANE (UNII: 918X1OUF1E)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
HYALURONIC ACID (UNII: S270N0TRQY)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
SALIX ALBA BARK (UNII: 205MXS71H7)
TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
XANTHAN GUM (UNII: TTV12P4NEE)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:83493-150-01	50 mL in 1 TUBE; Type 0: Not a Combination Product	03/01/2023

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M020	03/01/2023

Labeler - Krave Beauty, LLC (086662891)

Beet the sun lightweight sunscreen broad spectrum spf 40 pa+++