SUN BUM DAILY FACE LIQUID SUNSCREEN MOISTURIZER BROAD SPECTRUM SPF 50- avobenzone, homosalate, octisalate, octocrylene lotion

Sun Bum Daily Face Liquid Sunscreen Moisturizer Broad Spectrum SPF 50 by

Drug Labeling and Warnings

Sun Bum Daily Face Liquid Sunscreen Moisturizer Broad Spectrum SPF 50 by is a Otc medication manufactured, distributed, or labeled by Sun Bum, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Avobenzone 3%, Homosalate 9%, Octisalate 5%, Octocrylene 10%

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

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 immediately.

Warnings

Keep Out Of Reach Of Children

Directions

shake well before use

apply liberally 15 minutes before sun exposure

reapply: after 80 minutes of swimming or sweating immediately after towel drying at least every 2 hours

children under 6 months of age: ask a doctor

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

Directions

shake well before use

apply liberally 15 minutes before sun exposure

Other information

protect this product from excessive heat and direct sun

Inactive ingredients

water, alcohol denat (10%)., butyloctyl salicylate, glycerin, propanediol, isododecane, acrylates/polytrimethylsiloxy-methacrylate copolymer, cocos nucifera (coconut) oil, triethyl citrate, acacia senegal gum, acrylates/C10-30 alkyl acrylate crosspolymer, ethylhexylglycerin, lysolecithin, methyl gluceth-20, phenoxyethanol, pullulan, sclerotium gum, silica, sodium polyacrylate, tetrahexyldecyl ascorbate, tocopherol, tocopheryl acetate, trisodium ethylenediamine disuccinate, xanthan gum

Questions?

1-877-978-6286

Primary Artwork

INGREDIENTS AND APPEARANCE

SUN BUM DAILY FACE LIQUID SUNSCREEN MOISTURIZER BROAD SPECTRUM SPF 50 
avobenzone, homosalate, octisalate, octocrylene lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69039-664
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	50 mg  in 1 mL
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	30 mg  in 1 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	90 mg  in 1 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	100 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
GLYCERIN (UNII: PDC6A3C0OX)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
ISODODECANE (UNII: A8289P68Y2)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
METHYL GLUCETH-20 (UNII: J3QD0LD11P)
COCOS NUCIFERA (COCONUT) OIL (UNII: Q9L0O73W7L)
ACACIA SENEGAL GUM (UNII: 5C5403N26O)
XANTHAN GUM (UNII: TTV12P4NEE)
ALCOHOL (UNII: 3K9958V90M)
SILICA (UNII: ETJ7Z6XBU4)
WATER (UNII: 059QF0KO0R)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q)
PROPANEDIOL (UNII: 5965N8W85T)
BUTYL ACRYLATE/METHYL METHACRYLATE/TRIMETHYLSILOXYMETHACRYLATE COPOLYMER (UNII: Y3BP59PMD3)
TOCOPHEROL (UNII: R0ZB2556P8)
LYSOPHOSPHATIDYLCHOLINE, SOYBEAN (UNII: CQD833204Z)
SCLEROTIUM GUM (UNII: 2X51AD1X3T)
PULLULAN (UNII: 8ZQ0AYU1TT)
ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69039-664-02	1 in 1 CARTON	03/01/2024
1	NDC: 69039-664-01	50 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	03/01/2024

Labeler - Sun Bum, LLC (028642574)