FDA.reportPublic FDA data

AVOBENZONE,HOMOSALATE,OCTISALA,OCTOCRYLENETE,

Manufacturer
Innovation Labs, Inc.
Effective date
2024-01-24
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:12:37

Label at a glance#

ProductHello Sunday. The Everyday One. Broad Spectrum SPF 50 Sunscreen SPF 50 PA UVB UVA Face Moisturizer
Active ingredientAVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE
Label structure10 sections

Indications and uses

helps prevent sunburn if used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin ageing caused by the sun.

Dosage and administration

Apply generously on dry skin (we recommend 5 pumps, enough to cover your face, neck and ears) 15 minutes before sun exposure and as a last step in your skincare routine (before makeup). 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 ageing. To decrease this risk, regularly use...

Label contents#

Full prescribing information#

Active Ingredients:

OTC - ACTIVE INGREDIENT SECTION

Avobenzone 3%
Homosalate 7%
Octisalate 5%
Octocrylene 10%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Uses:

INDICATIONS & USAGE SECTION

  • helps prevent sunburn
  • if used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin ageing caused by the sun.

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

on damaged or broken skin

Stop use and ask a doctor

OTC - STOP USE SECTION

if rash occurs

WHen using this product,

OTC - WHEN USING SECTION

keep out of eyes. Rinse with water to remove.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • Apply generously on dry skin (we recommend 5 pumps, enough to cover your face, neck and ears) 15 minutes before sun exposure and as a last step in your skincare routine (before makeup).
  • 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 ageing. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and others 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

-Children under 6 onths of age: Ask a doctor.

Other Information

OTHER SAFETY INFORMATION

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

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, C12-15 Alkyl Benzoate, Glycerin, Cetearyl Alcohol, Glyceryl Stearate, Silica, Sodium Hyaluronate, Glycine Soja (Soybean) oil, Acrylates/C12-22 Alkyl Methacrylate Copolymer, Ethyl Ferulate, Tocopheryl Acetate, Tetrahexyldecyl, Ascorbate, Oryza Satina (Rice) Germ Extract, Caesalpinia Spinosa Fruit Pod Extract, Helianthus Annuus (Sunflower) Sprout Extract, Sodium Phytate, Maltodextrin, Moringa Oleifera Seed Extract, Hydroxyacetophenone, Sodium Stearoyl Glutamate, 1,2-Hexanediol, Caprylyl Glycol, Xanthan Gum, Polyglyceryl-3 Disostearate, Pentylene Glycol, Acrylates/C10-30Alkyl Acrylate Crosspolymer, Sodium Hydroxide

Questions or comments?

OTC - QUESTIONS SECTION

1-888-426-0695

Monday - Friday, 9 a.m. - 5 p.m. EST

73284 Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

73284 Innovation Labs Inc73284 Innovation Labs Inc

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 22 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73284-52173284-521-00

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 20 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ALKYL (C12-15) BENZOATEA9EJ3J61HQIACT
GLYCERINPDC6A3C0OXIACT
CETOSTEARYL ALCOHOL2DMT128M1SIACT
GLYCERYL MONOSTEARATE230OU9XXE4IACT
SILICON DIOXIDEETJ7Z6XBU4IACT
HYALURONATE SODIUMYSE9PPT4THIACT
SOYBEAN OIL241ATL177AIACT
ETHYL FERULATE5B8915UELWIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
TETRAHEXYLDECYL ASCORBATE9LBV3F07AZIACT
ASCORBIC ACIDPQ6CK8PD0RIACT
RICE GERM7N2B70SFEZIACT
CAESALPINIA SPINOSA FRUIT PODEXY4496LWDIACT
HELIANTHUS ANNUUS SPROUT4P26HG1S5WIACT
PHYTATE SODIUM88496G1ERLIACT
AVOBENZONEG63QQF2NOXACTIB
HOMOSALATEV06SV4M95SACTIB
OCTISALATE4X49Y0596WACTIB
OCTOCRYLENE5A68WGF6WMACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
0f51f10c-0ea2-9d3b-e063-6394a90a89eb6756c9ed-91c0-4aa6-a8e3-417a3420c8c32024-01-24WarningsExact identifier
spl id: 0f51f10c-0ea2-9d3b-e063-6394a90a89eb
spl set id: 6756c9ed-91c0-4aa6-a8e3-417a3420c8c3

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.