FDA.reportPublic FDA data

SnugZ SPF 50 Sunscreen Spry

Product NDC
76309-525
11-digit product format
763090525
Labeler code
76309
Product ID
76309-525_47209b8d-8e8b-e73a-e063-6394a90ae015
Type
HUMAN OTC DRUG
Nonproprietary name
SPF 50 Sunscreen Spray
Dosage form
SPRAY
Route
TOPICAL
Labeler
SnugZ USA
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2019-06-01
Substance
HOMOSALATE; OCTISALATE; OCTOCRYLENE; AVOBENZONE
Active strength
4.2; 1.4; 2.8; .84 g/28mL; g/28mL; g/28mL; g/28mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product
Yes
Brand name base
SnugZ SPF 50 Sunscreen Spry
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
HOMOSALATE4.2 g/28mL
OCTISALATE1.4 g/28mL
OCTOCRYLENE2.8 g/28mL
AVOBENZONE.84 g/28mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 4 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
V06SV4M95SInternal UNII lookup
4X49Y0596WInternal UNII lookup
5A68WGF6WMInternal UNII lookup
G63QQF2NOXInternal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
9390ea21-9f9f-14e2-e053-2a95a90ac577Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76309-525-10SnugZ SPF 50 Sunscreen Spry10 mL in 1 BOTTLE, SPRAYSPRAY107
76309-525-71SnugZ SPF 50 Sunscreen Spry28 mL in 1 BOTTLE, SPRAYSPRAY287

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76309-525SNUGZ SPF 50 SUNSCREEN SPRY (SPF 50 SUNSCREEN SPRAY) SPRAY [SNUGZ USA]6Current NDC, Legacy NDC, 2 package rows20241228_9390ea21-9f9f-14e2-e053-2a95a90ac577.zip

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 87 of 353 · 7,049 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
CabanaMilk Mineral Barrier Fluid SPF 50ZINC OXIDENAKED SUNDAYS PTY LTD47d0fe4d-ad21-1004-e063-6394a90a9c192026-01-07WarningsExact identifier
application number: M020
CENTELLA RELIEF SOOTHING SUNSCREENAVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENEIUNIK Co., Ltd.47d170e3-dd76-d413-e063-6294a90ae8e42026-01-07WarningsExact identifier
application number: M020
Round Lab Birch Juice Mild-Up UVLOCK Sunscreen SPF50 Broad SpectrumZINC OXIDESEORIN COMPANY Co., Ltd.1e7cc417-3c57-c87c-e063-6394a90a670b2026-01-07WarningsExact identifier
application number: M020
Proactiv Clear Skin SPF 30AVOBENZONE, OCTISALATE, AND OCTOCRYLENEAlchemee, LLCb0aa7ff0-f712-486f-aaaf-f88fed3b5cd12026-01-07WarningsExact identifier
application number: M020
Daily Hydrating Mineral Body Sunscreen Broad Spectrum SPF 30 SunscreenZINC OXIDEOak Essentials, LLC47d37f44-10b2-214f-e063-6294a90a5abc2026-01-07WarningsExact identifier
application number: M020
PLUMSCREEN SPF 31ZINC OXIDELe Prunier Farms, Inc.e20eb996-2b64-6bd0-e053-2a95a90a4f922026-01-07WarningsExact identifier
application number: M020
BETA-GLUCAN MILD SUNSCREENTITANIUM DIOXIDE, ZINC OXIDEIUNIK Co., Ltd47d6ad8b-1081-ee21-e063-6294a90a0e632026-01-07WarningsExact identifier
application number: M020
Koobarra Mineral Face Sunscreen SPF 50ZINC OXIDE SUNSCREENVEGANIC SKN LIMITED37cf8143-99f2-cca5-e063-6394a90a19a82026-01-07WarningsExact identifier
application number: M020
Solar Swipe Mineral Sunscreen SPF50SOLAR SWIPE MINERAL SUNSCREEN SPF50Guangzhou Fantesy Biotechnology Co.,Ltd47d75d61-5295-3eab-e063-6394a90a01c12026-01-07WarningsExact identifier
application number: M020
LUXURY SUN RITUAL PORE SMOOTHING SPF 30 SUNSCREENZINC OXIDEJANE STREET LLCdbdd3e6a-f09d-90cf-e053-2a95a90a98a02026-01-07WarningsExact identifier
application number: M020
RENEWALUXE SPF 50 SunscreenRENEWALUXE SPF 50 SUNSCREENGuangzhou Fantesy Biotechnology Co.,Ltd1bc29960-5e73-e8ab-e063-6294a90a3f802026-01-06WarningsExact identifier
application number: M020
ULTRA VIOLETTE VELVET SCREEN BLURRING MINERAL SKINSCREENSPF50Wild Child Laboratories PTY Ltd2767ba3e-7434-d474-e063-6294a90aa4ff2026-01-06WarningsExact identifier
application number: M020
ULTRA VIOLETTE SPF ON THE GLOW Duo Pack KitSPF 50Grace And Fire USA Inc.47b7da8a-ea89-1402-e063-6294a90a23f92026-01-06WarningsExact identifier
application number: M020
Hawaiian Blend Essential Zinc SPF 30ZINC OXIDE, TITANIUM DIOXIDEThe Islander Group5a6e622f-2c00-406a-8860-d7081656f5972026-01-06WarningsExact identifier
application number: M020
SHISEIDO SYNCHRO SKIN LASTING Liquid FOUNDATION Neutral 5OCTINOXATE AND TITANIUM DIOXIDESHISEIDO AMERICAS CORPORATION66c22f17-5418-42ff-97b2-33fa10f5eac32026-01-06WarningsExact identifier
application number: M020
SHISEIDO BENEFIANCE WRINKLERESIST24 DAYAVOBENZONE, OCTINOXATE, AND OCTOCRYLENESHISEIDO AMERICAS CORPORATION7d9c0f81-005f-4223-940e-a64143db52752026-01-06WarningsExact identifier
application number: M020
SHISEIDO FUTURE Solution LX INFINITE TREATMENT PRIMERTITANIUM DIOXIDE, OCTINOXATE, AND ENSULIZOLESHISEIDO AMERICAS CORPORATIONff088b0c-27c9-4ea8-bf94-6261378c71902026-01-06WarningsExact identifier
application number: M020
Drs. pharmacy sunscreen SPF 50 (physical filters)SUNSCREEN SPF 50OL PHARMA TECH LLC. (Drs. Pharmacy)31e976a2-0623-0dca-e063-6394a90a08da2026-01-06WarningsExact identifier
application number: M020
SHISEIDO SYNCHRO SKIN SELF-REFRESHING TINT 115 Fair ShirakabaOCTINOXATE, OCTOCRYLENE, AND TITANIUM DIOXIDESHISEIDO AMERICAS CORPORATION26151cf4-0fee-4a42-92fd-4d7b9cef83812026-01-06WarningsExact identifier
application number: M020
Drs. pharmacy sunscreen SPF 50 (physical filters)SUNSCREEN SPF 50OL PHARMA TECH LLC. (Drs. Pharmacy)315a5ca4-4536-d585-e063-6294a90a1c502026-01-06WarningsExact identifier
application number: M020

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
76309-525-107630905251010 mL in 1 BOTTLE, SPRAY (76309-525-10) 10 ml2019-06-010000-00-00NoNoCurrent
76309-525-717630905257128 mL in 1 BOTTLE, SPRAY (76309-525-71) 28 ml2019-06-010000-00-00NoNoCurrent