FDA.reportPublic FDA data

BRIGHTER DAY BROAD SPECTRUM

Manufacturer
SQN Lab
Effective date
2022-01-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:46:25

Label at a glance#

ProductBRIGHTER DAY BROAD SPECTRUM SPF 30 SUNSCREEN
Active ingredientZINC OXIDE
Label structure9 sections

Dosage and administration

APPLY LIBERALLY 15 MINUTES BEFORE SUN EXPOSURE. CHILDREN UNDER 6 MONTHS OF AGE: ASK A DOCTOR. USE A WATER-RESISTANT SUNSCREEN IF SWIMMING OR SWEATING. REAPPLY AT LEAST EVERY 2 HOURS. SUN PROTECTION MEASURES. SPENDING TIME IN THE SUN INCREASES YOUR RISK OF SKIN CANCER AND EARLY AGING. TO DECREASE THE RISK, REGULARLY USE A SUNSCREEN WITH A BROAD SPECTRUM SPF VALUE OF 15 OR HIGHER AND OTHER SUN PROTECTION MEASURES IN...

Storage and handling

PROTECT THE PRODUCT IN THIS CONTAINER FROM EXCESSIVE HEAT AND DIRECT SUN.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

ZINC OXIDE

PURPOSE

OTC - PURPOSE SECTION

SUNSCREEN

USE

INDICATIONS & USAGE SECTION

HELPS PREVENT SUNBURN

WARNINGS

WARNINGS SECTION

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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN. IF PRODUCT IS SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

  • APPLY LIBERALLY 15 MINUTES BEFORE SUN EXPOSURE.
  • CHILDREN UNDER 6 MONTHS OF AGE: ASK A DOCTOR.
  • USE A WATER-RESISTANT SUNSCREEN IF SWIMMING OR SWEATING.
  • REAPPLY AT LEAST EVERY 2 HOURS.
  • SUN PROTECTION MEASURES.
    SPENDING TIME IN THE SUN INCREASES YOUR RISK OF SKIN CANCER AND EARLY AGING. TO DECREASE THE 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 10:00 A.M. - 2 P.M.
  • WEAR LONG-SLEEVED SHIRTS, PANTS, HATS, AND SUNGLASSES.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

WATER, BUTYLENE GLYCOL, CAPRYLIC/CAPRIC TRIGLYCERIDE, DIETHYLHEXYL 2,6-NAPHTHALATE, HYDROXYETHYL ACRYLATE/SODIUM, ACRYLOYLDIMETHYL TAURATE COPOLYMER, SODIUM OLIVATE, XYLITYLGLUCOSIDE, ANHYDROXYLITOL, TRIETHOXYCAPRYLYLSILANE, XYLITOL,PENTYLENE GLYCOL, CITRIC ACID, TOCOPHEROL, CAMELLIA SINENSIS LEAF OIL, DIMETHICONE, PHENOXYETHANOL, ETHYLHEXYLGLYCERIN, IRON OXIDES.

OTHER INFORMATION

STORAGE AND HANDLING SECTION

  • PROTECT THE PRODUCT IN THIS CONTAINER FROM EXCESSIVE HEAT AND DIRECT SUN.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

01b UC_Brighter Day SPF 30_60mL01b UC_Brighter Day SPF 30_60mL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
82495-101-112025-01-30C16284748780-12cef2736-859f-d83d-e063-dadaa90ab31fSQN - BRIGHTER DAY BROAD SPECTRUM SPF30 (82495-101)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82495-101-11BRIGHTER DAY BROAD SPECTRUMSPF 30 SUNSCREEN1 in 1 BOXLOTION11
82495-101-11BRIGHTER DAY BROAD SPECTRUMSPF 30 SUNSCREEN50 mL in 1 TUBELOTION501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82495-101BRIGHTER DAY BROAD SPECTRUM SPF 30 SUNSCREEN (ZINC OXIDE) LOTION [SQN LAB]1Legacy NDC, 2 package rows20220106_d4dc1f89-7433-ae35-e053-2a95a90a5bfa.zip

Products#

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

DailyMed product names page 1 of 1 · 20 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82495-10182495-101-11

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 19 matching rows.

Name, UNII, Kind table
NameUNIIKind
DIETHYLHEXYL 2,6-NAPHTHALATEI0DQJ7YGXMIACT
TOCOPHEROLR0ZB2556P8IACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
WATER059QF0KO0RIACT
MEDIUM-CHAIN TRIGLYCERIDESC9H2L21V7UIACT
DIMETHICONE92RU3N3Y1OIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%)86FQE96TZ4IACT
SODIUM OLEATE399SL044HNIACT
XYLITYLGLUCOSIDEO0IEZ166FBIACT
ANHYDROXYLITOL8XWR7NN42FIACT
XYLITOLVCQ006KQ1EIACT
PENTYLENE GLYCOL50C1307PZGIACT
PHENOXYETHANOLHIE492ZZ3TIACT
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
FERRIC OXIDE RED1K09F3G675IACT
TEA LEAF OILVC855RRT77IACT
ZINC OXIDESOI2LOH54ZACTIB
TRIETHOXYCAPRYLYLSILANELDC331P08EIACT

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
d4dc10ff-6ae6-45d3-e053-2995a90aae89d4dc1f89-7433-ae35-e053-2a95a90a5bfa2022-01-05WarningsExact identifier
spl id: d4dc10ff-6ae6-45d3-e053-2995a90aae89
spl set id: d4dc1f89-7433-ae35-e053-2a95a90a5bfa

Reported adverse events (FAERS/openFDA)#

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