FDA.reportPublic FDA data

Sunscreen

Manufacturer
Rite Aid Corporation | Nice-Pak Products, LLC
Effective date
2026-01-30
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
monthly-update
Hydrated at
2026-06-03 17:55:59

Label at a glance#

ProductSunscreen
Active ingredientAVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE
Label structure14 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 aging caused by the sun

Dosage and administration

apply liberaly 15 minutes before sun exposure apply to all skin exposed to the sun reapply: after 80 minutes of swimming or sweating immediately after towel drying at least every 2 hours 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 Broad Spectrum SPF value of 15 or higher and other sun protection...

Label contents#

Full prescribing information#

active ingredients

OTC - ACTIVE INGREDIENT SECTION

Avobenzone 3%

Homosalate 10%

Octisalate 5%

Octocrylene 6%

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 aging caused by the sun

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

  • on damaged or broken skin

When using this product

OTC - WHEN USING SECTION

  • keep out of eyes.  Rinse with water to remove.

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • rash occurs

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • apply liberaly 15 minutes before sun exposure
  • apply to all skin exposed to the sun
  • reapply:
  • after 80 minutes of swimming or sweating
  • immediately after towel drying
  • at least every 2 hours
  • 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 Broad Spectrum SPF value of 15 or higher and other sun protection measures including:
  • limit time in the sun, especialy from 10  a.m. -2 p.m.
  • wear long-sleeved shirts, pants, hats and sunglasses
  • children under 6 months 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, silica, dimethicone, potassium cetyl phosphate, benzyl alcohol, beeswax, glyceryl stearate, PEG-100 stearate, caprylyl methicone, cetyl dimethicone, dimethicone/PEG-10/15 crosspolymer, sodium polyacrylate, behenyl alcohol, xanthan gum, glycerin, pentylene glycol, acrylates/C12-22 alkyl methacrylate copolymer, ethylhexyl stearate, chlorphenesin, disodium EDTA, fragrance, diethylhexyl 2,6-naphthalate, BHT, trideceth-6

Disclaimers

SPL UNCLASSIFIED SECTION

May stain or damage some fabrics or surfaces.

*This product is not manufacturedor distributed by Johnson & Johnson Consumer Inc., distributor of Neutrogena Ultra Sheer Dry-Touch Sunscreen Broad Spectrum SPF 30.

ADVERSE REACTION

ADVERSE REACTIONS SECTION

DISTRIBUTED BY: RITE AID

30 HUNTER LANE

CAMP HILL, PA 17011

www.riteaid.com

look great feel great

100% GUARANTEE or your money back

principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

daylogic™

FREE FROM OXYBENZONE - PHTHALATES

sheer

touch

SUNSCREEN LOTION

BROAD SPECTRUM SPF 30

UVA/UVB Protection

Water Resistant (80 minutes)

Non-greasy

Clean & Lightweight Feel

SPF 30

COMPARE TO NEUTROGENA ®ULTRA SHEER SUNSCREEN BROAD SPECTRUM SPF 30*

3 FL OZ (88 mL)

image descriptionimage description

Products#

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

DailyMed product names page 1 of 1 · 29 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
11822-191411822-1914-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 27 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
DIMETHICONE92RU3N3Y1OIACT
POTASSIUM CETYL PHOSPHATE03KCY6P7UTIACT
BENZYL ALCOHOLLKG8494WBHIACT
YELLOW WAX2ZA36H0S2VIACT
GLYCERYL MONOSTEARATE230OU9XXE4IACT
PEG-100 STEARATEYD01N1999RIACT
CAPRYLYL TRISILOXANEQ95M2P1KJLIACT
CETYL DIMETHICONE 1505L694Y0T22IACT
DIMETHICONE/PEG-10/15 CROSSPOLYMER21AS8B1BSSIACT
SODIUM POLYACRYLATE (8000 MW)285CYO341LIACT
DOCOSANOL9G1OE216XYIACT
XANTHAN GUMTTV12P4NEEIACT
GLYCERINPDC6A3C0OXIACT
PENTYLENE GLYCOL50C1307PZGIACT
ALLYL METHACRYLATEG2IG50653ZIACT
ETHYLHEXYL STEARATEEG3PA2K3K5IACT
CHLORPHENESINI670DAL4SZIACT
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT
DIETHYLHEXYL 2,6-NAPHTHALATEI0DQJ7YGXMIACT
BUTYLATED HYDROXYTOLUENE1P9D0Z171KIACT
TRIDECETH-63T5PCR2H0CIACT
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
4ce8fd92-2410-a07a-e063-6294a90abbd077bbc019-46ad-460a-87ff-6456ca20da6c2026-03-13Warnings, Adverse reactionsExact identifier
spl set id: 77bbc019-46ad-460a-87ff-6456ca20da6c

Reported adverse events (FAERS/openFDA)#

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